Antitumoral compounds

ABSTRACT

New spisulosine derivatives of use in treating tumors are of the formula (I) wherein: each X is the same or different, and represents H, OH, OR′, SH, SR′, SOR′, SO 2 R′, NO 2 , NH 2 , NHR′, N(R′) 2 , CN, halogen, C(═O)H, C(═O)CH 3 , CO 2 H, CO 2 CH 3 , substituted or unsubstituted C 1 –C 18  alkyl, substituted or unsubstituted C 2 –C 18  alkenyl, substituted or unsubstituted C 2 –C 18  alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic, or two groups X may together form ═O; Y is NR 1 , OR 1 , PR 1 , SR 1 , or halogen, wherein the number of substituents R 1  is selected to suit the valency and each R 1  is independently selected of H, OH, C(═O)R′, P(═O)R′R″, substituted or unsubstituted C 1 –C 18  alkyl, substituted or unsubstituted C 2 –C 18  alkenyl, substituted or unsubstituted C 2 –C 18  alkynyl, substituted or unsubstituted aryl, and wherein the dotted line indicates an optional double bond; each Z is the same different, and represents H, OH, OR′, SH, SR′, SOR′, SO 2 R′, NO 2 , NH 2 , NHR′, N(R′) 2 , NHC(O)R′, CN, halogen, C(═O)H, C(═O)CH 3 , CO 2 H, CO 2 CH 3 , substituted or unsubstituted C 1 –C 18  alkyl, substituted or unsubstituted C 2 –C 18  alkenyl, substituted or unsubstituted C 2 –C 18  alkenyl, substituted or unsubstituted C 2 –C 18  alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic, or two groups Z may together form ═O; z is 0 to 25; y is to 0 to 20; R 2  is H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, S(═O) 2 R′, substituted or unsubstituted C 1 –C 18  alkyl, substituted or unsubstituted C 2 –C 18  Alkenyl, substituted or unsubstituted C 2 –C 18  alkynyl, substituted or unsubstituted aryl; R 3  is H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, S(═O) 2 R′, substituted or unsubstituted C 1 –C 18  alkyl, substituted or unsubstituted C 2 –C 18  alkenyl, substituted or unsubstituted C 2 –C 18  alkynyl, substituted or unsubstituted aryl; each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO 2 , NH 2 , SH, CN, halogen, ═O, C(═O)H, C(═O)CH 3 , CO 2 H, CO 2     CH     3 , substituted or unsubstituted C 1 –C 18  alkyl, substituted or unsubstituted C 1 –C 18  alkoxy, substituted or unsubstituted C 2 –C 18  alkenyl, substituted or unsubstituted C 2 –C 18  alkynl, substituted or unsubstituted aryl; there may be one or more unsaturations in the hydrocarbon backbone defined by the chain (II) and salts thereof; with the exception of a C 16 –C 24  2-amino-3-hydroxyalkane or a C 16 –C 24  2-amino-3-hydroxyalkene

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority from PCT/GB01/02487 filed on Jun. 6, 2001, which claims priority from United Kingdom Patent Application No. GB 0013783.6, filed on Jun. 6, 2000, United Kingdom Patent Application No. GB 0102472.8 filed on Jan. 31, 2001, and United Kingdom Patent Application No. GB 0104732.3, all of which are incorporated herein by reference in their entirety.

FIELD OF THE INVENTION

The present invention relates to new antitumoral derivatives of spisulosine-285.

BACKGROUND OF THE INVENTION

Spisulosine 285 is a bioactive compound that has been found to possess specific antitumor activity, described in the International Patent WO 99/52521. In the same patent specification are also described sphingoid-type bases spisulosines 299 and 313 and some sphingosine analogs.

-   -   1 (spisulosine-285) n=14     -   2 (spisulosine-299) n=15     -   3 (spisulosine-313) n=16

-   -   sphingosine, n=12 and nonadeca-4-sphingenine, n=13; and

Spisulosines 285, 299 and 313 were isolated from Spisula polynyma, an edible clam originally isolated from samples found off the coast of Japan. The compound we call spisulosine 285 and the syn diastereoisomer were first synthetized by Croatian researchers in the determination of absolute configurations of lipid bases with two or more asymmetric carbon atoms (Prostenik, M.; Alaupovic, P. Croat. Chem. Acta. 1957, 29, 393).

SUMMARY OF THE INVENTION

The present invention is directed to analogs of the spisulosine family having the following formulae I and II:

Wherein the substituent groups defined by R₁, R₂ and R₃ are each independently selected of H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl. Wherein each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ynyl, substituted or unsubstituted aryl.

R₂ can be independently an internal salt. Preferred internal salts are formed using any kind of mineral or organic acid such as hydrochloric acid, hydrobromic acid, tartaric acid, succinic acid, etc.

Wherein the substituent groups defined by X₁, X₂ and X₃ are independently selected of H, OH, OR′, SH, SR′, SOR′, SO₂R′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic. Wherein substituent groups defined by R′ are each independently selected from the group consisting of H, OH, OR′, SH, SR′, SOR′, SO₂R′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic.

Wherein x and y can be between 0 and 20. Preferably x is in the range 8 to 16, more preferably 10, 11, 12, 13 or 14. Preferably y is 0, 1 or 2. Currently the most preferred is that x is 11, 12 or 13, and y is 0 or 1.

Wherein the dotted line is one or several double bonds placed in any particular position of the side chain.

Wherein the stereochemistry of the groups OR₁ and NR₂R₃ in formula I can be independently syn or anti.

Wherein the group defined by Y in formula II is independently selected from the group consisting of N, O, P, S, halogen. Wherein the dotted line is a single or double bond. Wherein R₁ is independently selected of H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl. Wherein each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl.

In one aspect, we provide compounds of the formula I:

Wherein the substituent groups defined by R₁, R₂ and R₃ are each independently selected of H, C(═O)R′, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl.

R₂ can be independently an internal salt. Preferred internal salts are formed using any kind of mineral or organic acid such as hydrochloric acid, hydrobromic acid, tartaric acid, succinic acid, etc.

Wherein each of the R′ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl.

Wherein X₁, X₂ and X₃ are independently selected of H, OH, OR′, SH, SR′, SOR′, SO₂R′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic.

Wherein substituent groups defined by R′ are each independently selected from the group consisting of H, OH, OR′, SH, SR′, SOR′, SO₂R′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic.

Wherein x and y can be between 0 and 20.

Wherein the dotted line is one or several double bonds placed in any particular position of the side chain.

Wherein the stereochemistry of the groups OR₁ and NR₂R₃ can be independently syn or anti.

Suitable halogen substituents in the compounds of the present invention include F, Cl, Br and I.

Alkyl groups preferably have from 1 to about 12 carbon atoms, more preferably 1 to about 8 carbon atoms, still more preferably 1 to about 6 carbon atoms, and most preferably 1, 2, 3 or 4 carbon atoms. Methyl, ethyl and propyl including isopropyl are particularly preferred alkyl groups in the compounds of the present invention. As used herein, the term alkyl, unless otherwise modified, refers to both cyclic and noncyclic groups, although cyclic groups will comprise at least three carbon ring members.

Preferred alkenyl and alkynyl groups in the compounds of the present invention have one or more unsaturated linkages and from 2 to about 12 carbon atoms, more preferably 2 to about 8 carbon atoms, still more preferably 2 to about 6 carbon atoms, even more preferably 1, 2, 3 or 4 carbon atoms. The terms alkenyl and alkynyl as used herein refer to both cyclic and noncyclic groups, although straight or branched noncyclic groups are generally more preferred.

Preferred alkoxy groups in the compounds of the present invention include groups having one or more oxygen linkages and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferably 1 to about 6 carbon atoms, and most preferably 1, 2, 3 or 4 carbon atoms.

Preferred alkylthio groups in the compounds of the present invention have one or more thioether linkages and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferably 1 to about 6 carbon atoms. Alkylthio groups having 1, 2, 3 or 4 carbon atoms are particularly preferred.

Preferred alksulfinyl groups in the compounds of the present invention include those groups having one or more sulfoxide (SO) groups and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferably 1 to about 6 carbon atoms. Alkylsulfinyl groups having 1, 2 3 or 4 carbon atoms are particularly preferred.

Preferred alkylsulfonyl groups in the compounds of the present invention include those groups having one or more sulfonyl (SO₂) groups and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferably 1 to about 6 carbon atoms. Alkylsulfonyl groups having 1, 2, 3 or 4 carbon atoms are particularly preferred.

Preferred aminoalkyl groups include those groups having one or more primary, secondary and/or tertiary amine groups, and from 1 to about 12 carbon atoms, more preferably 1 to about 8 carbon atoms, still more preferably 1 to about 6 carbon atoms, even more preferably 1, 2, 3 or 4 carbon atoms. Secondary and tertiary amine groups are generally more preferred than primary amine moieties.

Suitable heteroaromatic groups in the compounds of the present invention contain one, two or three heteroatoms selected from N, O or S atoms and include, e.g., coumarinyl including 8-coumarinyl, quinolinyl including 8-quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl and benzothiazolyl. Suitable heteroalicyclic groups in the compounds of the present invention contain one, two or three heteroatoms selected from N, O or S atoms and include, e.g., tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl groups.

Suitable carbocyclic aryl groups in the compounds of the present invention include single and multiple ring compounds, including multiple ring compounds that contain separate and/or fused aryl groups. Typical carbocyclic aryl groups contain 1 to 3 separate or fused rings and from 6 to about 18 carbon ring atoms. Specifically preferred carbocyclic aryl groups include phenyl including substituted phenyl such as 2-substituted phenyl, 3-substituted phenyl, 2, 3-substituted phenyl, 2,5-substituted phenyl, 2,3,5-substituted and 2,4,5-substituted phenyl, including where one or more of the phenyl substituents is an electron-withdrawing group such as halogen, cyano, nitro, alkanoyl, sulfinyl, sulfonyl and the like; naphthyl including 1-naphthyl and 2-naphthyl; biphenyl; phenanthryl; and anthracyl.

References herein to substituted R′ groups in the compounds of the present invention refer to the specified moiety that may be substituted at one or more available positions by one or more suitable groups, e.g., halogen such as fluoro, chloro, bromo and iodo; cyano; hydroxyl; nitro; azido; alkanoyl such as a C1–6 alkanoyl group such as acyl and the like; carboxamido; alkyl groups including those groups having 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms and more preferably 1–3 carbon atoms; alkenyl and alkynyl groups including groups having one or more unsaturated linkages and from 2 to about 12 carbon or from 2 to about 6 carbon atoms; alkoxy groups having those having one or more oxygen linkages and from 1 to about 12 carbon atoms or 1 to about 6 carbon atoms; aryloxy such as phenoxy; alkylthio groups including those moieties having one or more thioether linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; alkylsulfinyl groups including those moieties having one or more sulfinyl linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; alkylsulfonyl groups including those moieties having one or more sulfonyl linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; aminoalkyl groups such as groups having one or more N atoms and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; carbocylic aryl having 6 or more carbons, particularly phenyl (e.g., R being a substituted or unsubstituted biphenyl moiety); and aralkyl such as benzyl. Substituent groups may themselves be substituted, as in a trifluoromethylcinnamoyl group or an aminoacid acyl group such as with valine or Boc-valine.

1. The present invention notably provides compounds of formula:

wherein: each X is the same or different, and represents H, OH, OR′, SH, SR′, SOR′, SO₂R′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic, or two groups X may together form ═O;

Y is NR₁, OR₁, PR₁, SR₁, or halogen, wherein the number of substituents R₁ is selected to suit the valency and each R₁ is independently selected of H, OH, C(═O)R′, P(═O)R′R″, S(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, and wherein the dotted line indicates an optional double bond such that Y can also be ═O or ═N—OH or the group Y with NR₂R₃ and the intervening atoms can form a heterocycle;

each Z is the same or different, and represents H, OH, OR′, SH, SR′, SOR′, SO₂R′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic, or two groups Z may together form ═O;

-   -   z is 0 to 25;     -   y is 0 to 20;

R₂ and R₃ are the same or different and each is H, C(═O)R′, C(=S)R′, P(═O)R′R″, S(═O)R′R″, S(═O)2R′, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl;

each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, NHR′, NR′R″, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₁–C₁₈ alkoxy, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl;

there may be one or more unsaturations in the hydrocarbon backbone defined by the chain:

and salts thereof.

Typically each X is H.

Typically Y is NR₁, OR₁, PR₁, or halogen, wherein the number of substituents R₁ is selected to suit the valency and each R₁ is independently selected of H, C(═O)R′, P(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, and wherein the dotted line indicates an optional double bond such that Y can also be ═O or ═N—OH, or the group Y with NR₂R₃ and the intervening atoms can form a heterocycle.

Typically Z represents H, NH₂, NHR′, N(R′)₂, halogen, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaromatic.

Typically z is 10 to 20.

Typically is 0 to 4.

Typically R₂ and R₃ are the same or different and each is H, C(═O)R′, C(=S)R′, S(═O)R′R″, S(═O)₂R′, substituted or unsubstituted C₁–C₁₈ alkyl;

Each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, NHR′, NR′R″, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₁–C₁₈ alkoxy, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl, the selection of respective classes of defintions being made as appropriate to suit the preferred defintions given subsequently.

Compounds of this invention extend to salts, notably pharmaceutically acceptable salts. Such salts may be formed with organic or inorganic acids, and examples are given in this text.

In one class of compounds of this invention, the hydrocarbon backbone defined by the chain:

is of the formula:

where x is 0 to 20 and the dotted line indicates one or more double bonds in the backbone. For example there can a double bond at the position shown by the dotted line. For example, the hydrocarbon backbone is of the formula:

where x and y are as defined.

A preferred group of compounds of this invention include those wherein the terminal group —C(X)₃ is —CH₃.

In another preferred class, there are no unsaturations in the hydrocarbon backbone.

For preference, z is from 10 to 19.

Suitable compounds include those where Y is OH, O(C═O)R′ where R′ is optionally halogen-substituted alkyl, OR′ where R′ is alkyl, halogen, OP(═O)R′₂ where R′ is alkoxy, NH₂, ═O, ═NOH, or the group Y when OH with NR₂R₃ and the intervening atoms form a heterocycle of formula:

If desired, R₂ and R₃ are the same. Typically at least one of R₂ and R₃ is alkyl; alkyl substituted by aryl; hydrogen; C(═O)R′ where R′ is alkyl or alkoxy, halogen-substituted alkyl, optionally substituted amino-substitued alkyl, aryloxy, alkoxy, optionally substituted aryl-substituted alkenyl; (C═S)NHR′ where R′ is aryl; (C═O)NHR′ where R′ is aryl or alkyl; SO₂R′ where R′ is alkyl, or (C═O)R′ where R′ is optionally substituted aminoalkyl thereby giving an optionally substituted aminoacid acyl group.

In preferred compounds, y is 0 to 3.

The terminal group —C(Z)₃ can be —CH₃.

The stereochemistry is usually:

Notable preferred compounds meet two or more of the following criteria:

-   (a) the terminal group —C(X)₃ is —CH₃; -   (b) z is 10, 11, 12, 13, 14, 15, 16, 17, 18 or 19 -   (c) the hydrocarbon backbone is of the formula:

where x is 12;

-   (d) Y is OR₁ where R₁ is H, methyl, acetyl, PO(OMe)2, COCF3 or Y is     Cl, NH₃ ⁺Cl—, ═O, ═NOH; -   (e) R₂ and R₃ are independently selected from the group consisting     of H, methyl, acetyl, benzyl, Boc, CSNHPh, CONHPh, CONH^(n)Bu,     SO₂Me, COCF₃, COCH═CHPh, COCH═CHPhCF₃, COC₁₅H₃₂, COCH(NHBoc)CHMe₂,     COCH(NH₃ ⁺Cl⁻)CHMe₂; -   (f) y is 0, 1, 2 or 3; -   (g) Z is the same or different, and represents H, F, methyl, ethyl,     hydroxyphenyl, amino, dibenzylamino or NH₃Cl; -   (h) the stereochemistry is

or

-   (i) the compound or salt is in the form of a salt.

At least one of the following criteria can apply:

-   (j) z is not 12, 13 or 14; -   (k) Y is not OH; -   (l) at least one of R₂ and R₃ is not hydrogen; -   (m) y is at least 1; -   (n) at least one Z is not hydrogen; -   (o) the compound or salt is in the form of a salt.

Preferred combinations of these criteria include (k) with (l), (k) with (n), (l) with (n), any of these with (i), any of these with (a), any of these with (b). Other preferred combinations which may be taken with or without these combinations include (d) taken with (k), (e) taken with (l), (g) taken with (n).

A preferred class of compounds is of the formula:

where z is 10 to 19;

Y is OR₁ where R₁ is H, methyl, acetyl, PO(OMe)₂, COCF₃ or Y is Cl, NH₃ ⁺Cl⁻, ═O, ═NOH;

R₂ and R₃ are independently selected from the group consisting of H, methyl, acetyl, benzyl, Boc, CSNHPh, CONHPh, CONH^(n)Bu, SO₂Me, COCF₃, COCH═CHPh, COCH═CHPhCF₃, COC₁₅H₃₂, COCH(NHBoc)CHMe₂, COCH(NH₃ ⁺Cl⁻)CHMe₂;

Z represents H, F, methyl, ethyl, hydroxyphenyl, amino, dibenzylamino or NH₃Cl.

Typical compounds of this invention include the following:

Antitumoral activities of these compounds include leukaemias, lung cancer, colon cancer, kidney cancer, prostate cancer, ovarian cancer, breast cancer, sarcomas and melanomas.

Another especially preferred embodiment of the present invention is pharmaceutical compositions useful as antitumor agents which contain as active ingredient a compound or compounds of the invention, including salts, as well as the processes for their preparation.

Examples of pharmaceutical compositions include any solid (tablets, pills, capsules, granules etc.) or liquid (solutions, suspensions or emulsions) with suitable composition or oral, topical or parenteral administration.

Administration of the compounds or compositions of the present invention may be any suitable method, such as intravenous infusion, oral preparation, intraperitoneal and intravenous preparation.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The compounds of the present invention can be prepared synthetically. The present invention includes the synthetic processes described in the following schemes. Scheme 1 illustrates the preparation of the different aldehydes used as starting materials for the synthesis of spisulosine derivatives.

Scheme 2 shows the preparation of spisulosine derivatives having the (2S,3R) configuration using the aldehyde derived from the corresponding L-aminoacid and Grignard reagents of different lengths.

Scheme 3 describes the synthesis of the enantiomeric form of the final products of spisulosine starting from the corresponding D-alanine derivative.

The methods for the synthesis of N-acetyl, O-methyl, 3-halo-3-deoxy and O-phosphate derivatives of spisulosine are outlined in Scheme 4.

Scheme 5 shows the preparation of the corresponding (2S,3S) diastereoisomers of spisulosine, in which the final diamine is prepared via the azide intermediate. Preparation of the diastereoisomeric form of this diamine is outlined in Scheme 6.

In addition, the methods for the synthesis of O-acetyl and O-trifluoroacetyl derivatives of spisulosine are shown in Scheme 6.

Other Spisulosines 285 and 299 derivatives are prepared following different procedures which are described in Scheme 7.

3-Keto derivatives of spisulosine and their corresponding oximes can be prepared as described in Scheme 8.

The enantiomeric form of ketone 126 is prepared from the appropriate aminoalcohol as indicated in Scheme 9.

The synthesis of the 1-fluoro derivative of spisulosine starting from D-erythrosphingosine is depicted in Scheme 10.

TABLE 1 Cytotoxicity of Spisulosine Analogs (IC50, Molar) Compound MW P388 A549 HT29 MEL28 DU145

285.51 3.50E−08 3.50E−08 3.50E−08 1.75E−07 3.50E−08

299.53 3.34E−08 3.34E−08 3.34E−08 3.34E−08 3.34E−08

313.56 3.19E−08 3.19E−08 3.19E−08 3.19E−07 3.19E−08

229.40 4.36E−07 2.18E−06 4.36E−07 2.18E−06 2.18E−06

243.43 4.11E−07 4.11E−07 4.11E−07 2.05E−06 4.11E−07

257.46 3.88E−07 1.94E−07 3.88E−07 3.68E−07 1.94E−07

293.92 3.40E−09 3.40E−09

451.73 NA NA NA NA NA

271.48 3.68E−08 3.68E−08 3.68E−08 3.68E−08 3.68E−08

307.94 3.25E−08 3.25E−08

360.55 2.77E−08 2.77E−08 2.77E−08 2.77E−08 2.77E−08

321.97 3.11E−08 3.11E−08 1.55E−08 3.11E−07 3.11E−08

479.78 NA NA NA NA NA

336.00 2.98E−08 2.98E−08

493.81 NA NA NA NA NA

350.02 1.43E−08 1.43E−08

327.59 1.53E−07 3.05E−07 3.05E−07 3.05E−07 3.05E−07

364.05 2.75E−08 2.75E−08

341.61 2.93E−07 NA 1.46E−06 NA 1.46E−06

355.64 1.41E−06 NA 2.81E−06 NA 2.81E−06

285.51 3.50E−09 3.50E−09

321.97 1.55E−08 1.55E−08

299.53 3.34E−08 3.34E−08 3.34E−08 3.34E−07 3.34E−08

336.00 2.98E−09 2.98E−09

313.56 3.19E−07 3.19E−07

350.02 2.86E−08 2.86E−08

327.59 3.05E−08 3.05E−08

364.05 2.75E−08 2.75E−08

313.56 1.59E−07 1.59E−07

350.02 2.86E−08 2.86E−08

313.56 NA NA

350.02 NA NA

364.05 NA NA

377.60 1.32E−06 1.32E−06

414.06 2.42E−07 2.42E−07

328.58 1.52E−06 1.52E−06

401.50 1.24E−06 1.24E−06

285.51 3.50E−07 3.50E−07 3.50E−07 3.50E−07 3.50E−07

327.55 NA NA NA NA NA

299.53 1.67E−06 1.67E−06

303.95 3.29E−07 3.29E−07 3.29E−07 3.29E−07 3.29E−07

393.54 1.27E−06 1.27E−06 1.27E−06 1.27E−06 1.27E−06

285.51 3.50E−07 3.50E−07 3.50E−07 3.50E−07 3.50E−07

299.53 3.34E−07 3.34E−07 3.34E−07 3.34E−07 3.34E−07

357.44 1.40E−06 1.40E−06

385.62 NA NA

495.54 2.02E−08 2.02E−08

427.66 NA NA NA NA NA

364.01 2.75E−07 2.75E−07 1.37E−07 2.75E−07 1.37E−07

357.44 2.80E−07 2.80E−07

313.56 3.19E−07 3.19E−07 3.19E−07 3.19E−07 3.19E−07

299.53 3.34E−07 3.34E−07 3.34E−07 3.34E−07 3.34E−07

420.70 NA NA NA NA NA

404.63 NA NA

384.64 NA NA

363.60 2.75E−08 2.75E−08

377.63 2.65E−07 2.65E−07

395.54 NA NA

477.52 NA NA

395.54 NA NA

415.65 NA NA

483.65 NA NA

539.96 NA NA

484.76 NA NA

421.10 NA NA

305.93 1.63E−07 1.63E−07 1.63E−07 3.27E−07 1.63E−07

319.95 3.13E−08 1.56E−07 3.13E−08 1.56E−07 3.13E−08

298.51 3.35E−07 3.35E−07 3.35E−07 3.35E−07 3.35E−07

333.98 1.50E−07 1.50E−07 1.50E−07 2.99E−07 1.50E−07

348.01 1.44E−07 1.44E−07 1.44E−07 2.87E−07 1.44E−07

333.98 2.99E−08 2.99E−08 2.99E−08 2.99E−07 2.99E−08

319.95 1.56E−07 1.56E−07 1.56E−07 3.13E−07 1.56E−07

325.49 NA NA NA NA NA

327.48 NA NA NA NA NA

301.48 3.32E−08 3.32E−08

303.50 3.29E−08 3.29E−08 3.29E−08 3.29E−07 3.29E−07 Methodology: after Berjeron et al, Biochem and Bioph Res. Comm., 1984, 121, 3, 848–854 NA=not active

TABLE 2 Cytotoxicity of Spisulosine Analogs (IC50, Molar) Solid Tumors Line

Bladder 5637 4.72E−08 6.34E−06 3.65E−08 Breast MX-1 1.95E−06 Colon HT-29 1.28E−07 6.43E−08 9.07E−06 2.64E−07 Gastric Hs746t 3.95E−07 Liver SK-HEP-1 2.97E−07 NSCL A549 8.57E−08 3.43E−08 9.79E−06 1.01E−05 Ovary SK-OV-3 7.02E−07 Pancreas PANC-1 1.67E−07 7.22E−07 8.64E−08 Pharynx FADU 2.49E−07 1.03E−08 8.12E−08 7.84E−08 Prostate PC-3 8.60E−08 4.9E−08 3.79E−07 Prostate DU-145 7.39E−08 9.86E−06 2.01E−07 Prostate LNCAP 4.44E−08 7.69E−06 7.15E−08 Renal 786-O 1.38E−07 SCL NCI-H187 1.63E−07 7.17E−06 NA Retinoblastoma Y-79 4.65E−06 NA NA Melanoma Mel-28 7.21E−06 NA 1.03E−05 Fibrosarcoma SW 694 NA 6.49E−06 1.04E−05 1.01E−05 Chondrosarcoma CHSA 1.80E−08 1.58E−06 9.65E−06 Osteosarcoma OSA-FH 1.83E−07 8.60E−06 NA Methodology: MTS. 4-Parameter Curve Fit w/SoftMax. Values are Molar NA = not active Solid Tumors Line

Bladder 5637 7.80E−06 3.26E−06 NA 2.99E−05 Breast MX-1 NA 2.84E−06 1.49E−05 Colon HT-29 9.11E−06 NA NA Gastric Hs746t NA Liver SK-HEP-1 NA NSCL A549 1.03E−05 4.90E−05 NA NA Ovary SK-OV-3 NA Pancreas PANC-1 1.86E−07 NA NA NA Pharynx FADU 2.25E−07 1.96E−05 NA NA Prostate PC-3 1.02E−05 Prostate DU-145 7.55E−08 NA Prostate LNCAP 6.35E−06 NA Renal 786-O NA 1.62E−07 NA SCL NCI-H187 7.29E−06 3.55E−06 Retinoblastoma Y-79 9.51E−06 1.21 E−05 Melanoma Mel-28 9.4E−06 NA NA NA Fibrosarcoma SW 694 7.57E−06 Chondrosarcoma CHSA 8.94E−06 NA NA NA Osteosarcoma OSA-FH 8.52E−06 NA NA 1.49E−05 Solid Tumors Line

Bladder 5637 NA 1.58E−06 1.45E−06 Breast MX-1 NA 1.72E−06 4.29E−06 Colon HT-29 NA NA Gastric Hs746t 1.62E−05 Liver SK-HEP-1 1.55E−05 NSCL A549 2.01E−05 NA Ovary SK-OV-3 NA Pancreas PANC-1 NA NA Pharynx FADU 1.43E−05 2.99E−06 3.96E−06 Prostate PC-3 2.18E−05 Prostate DU-145 4.95E−08 Prostate LNCAP NA Renal 786-O NA 5.98E−05 3.30E−06 SCL NCI-H187 Retinoblastoma Y-79 1.65E−06 Melanoma Mel-28 NA NA 2.54E−06 Fibrosarcoma SW 694 Chondrosarcoma CHSA NA NA 4.62E−06 Osteosarcoma OSA-FH NA NA Methodology: MTS. 4-Parameter Curve Fit w/SoftMax. Values are Molar NA = not active

TABLE 3 Cytotoxicity of Spisulosine Analogs (IC50, Molar) Leukemias/Lymphomas Line

ALL (Promyelocytic leukemia) HL-60 4.25E−07 ALL (Acute lymphobalstic) Molt 3 1.12E−06 7.61E−06 9.83E−09 CML (Chronic myelogenous) K562 7.84E−07 ALL (B-cell) CCRF-SB NA Leukemia (Hairy B-cell) Mo-B Leukemia (Plasma cell) ARH-77 6.82E−07 Lymphoma (T cell) H9 1.55E−06 Lymphoma (Cutaneous T cell) Hut 78 2.16E−06 1.06E−05 NA 8.81E−06 Lymphoma MC116 8.82E−06 1.09E−05 9.58E−06 (undifferentiated) Lymphoma (Burkitts B cell) RAMOS 2.14E−06 Lymphoma (Histiocytic) U-937 9.81E−07 2.98E−08 NA Lymphoma (B cell) CCRF-SB Lymphoma (B cell) MoB Lymphoma (Burkitts ascites) P3HR1 3.37E−06 Methodology: MTS. 4-Parameter Curve Fit w/SoftMax. Values are Molar NA = not active Leukemias/Lymphomas Line

ALL (Promyelocytic leukemia) HL-60 ALL (Acute lymphobalstic) Molt 3 3.76E−08 2.61E−05 NA CML (Chronic myelogenous) K562 0.001 ALL (B-cell) CCRF-SB Leukemia (Hairy B-cell) Mo-B Leukemia (Plasma cell) ARH-77 Lymphoma (T cell) H9 NA NA NA Lymphoma Hut 78 9.15E−06 (Cutaneous T cell) Lymphoma MC116 NA NA NA (undifferentiated) Lymphoma (Burkitts B cell) RAMOS NA NA Lymphoma U-937 NA NA (Histiocytic) Lymphoma (B cell) CCRF-SB Lymphoma (B cell) MoB Lymphoma (Burkitts P3HR1 ascites) Leukemias/Lymphomas Line

ALL (Promyelocytic leukemia) HL-60 1.29E−06 ALL (Acute lymphobalstic) Molt 3 1.43E−05 5.81E−07 CML (Chronic myelogenous) K562 ALL (B-cell) CCRF-SB Leukemia (Hairy B-cell) Mo-B Leukemia (Plasma cell) ARH-77 Lymphoma (T cell) H9 2.59E−06 5.98E−06 Lymphoma (Cutaneous T cell) Hut 78 Lymphoma (undifferentiated) MC116 NA NA Lymphoma (Burkitts B cell) RAMOS 1.65E−06 1.21E−06 Lymphoma (Histiocytic) U-937 NA NA Lymphoma (B cell) CCRF-SB Lymphoma (B cell) MoB Lymphoma (Burkitts ascites) P3HR1 Methodology: MTS. 4-Parameter Curve Fit w/SoftMax. Values are Molar NA = not active Experimental Section General Procedures

All solvents were reagent grade (used in work-ups) or HPLC grade (used as reaction and/or as purification solvent). Anhydrous solvents were used directly as supplied by the manufacturer. All other reagents were commercial compounds of the highest purity available. All amino acids and their derivatives used as starting materials were commercially available. Compounds 1 and 39 were described in the International Patent WO 99/52521. Analytical thin-layer chromatography (TLC) was performed on Merck silica gel aluminium sheets (60, F254) precoated with a fluorescent indicator. Visualization was effected using ultraviolet light (254 nm), phosphomolybdic acid (7% w/v) in 95% ethanol. Proton and carbon magnetic resonance spectra (¹H, ¹³C-NMR) were recorded on a Varian-300 (300 MHz) Fourier transform spectrometer, and chemical shifts were expressed in parts per million (ppm) relative to CHCl₃ as an internal reference (7.26 ppm for ¹H and 77.0 for ¹³C). Multiplicities are designated as singlet (s), doublet (d), doublet of doublets (dd), doublet of triplets (dt), triplet (t), quartet (q), quintet (quint), multiplet (m), and broad singlet (br s). Electrospray ionization mass spectra (ESI-MS) were obtained on a Hewlett Packard Series 1100 MSD. Flash column chromatography was carried out on E. Merck silica gel 60 (240–400 mesh) using the solvent systems listed under individual experiments.

EXAMPLES OF THE INVENTION

Illustrative examples of the synthesis of spisulosine derivatives according to the present invention are as follows:

Example 1 (S)-2-(N,N-Dibenzylamino)-propionaldehyde, 4

To a cold (−78° C.) solution of (COCl)₂ (2M in CH₂Cl₂, 2.47 mL, 4.94 mmol) in CH₂Cl₂ (8 mL), DMSO (0.70 mL, 9.89 mmol) was added dropwise. After stirring at −78° C. for 15 min, a solution of (S)-2-(N,N-dibenzylamino)-1-propanol (1.01 g, 3.96 mmol) in CH₂Cl₂ (10 mL) was added dropwise. The mixture was stirred at −78° C. for 1 h, and then Et₃N (2.76 mL, 19.78 mmol) was added. The reaction was warmed up to 0° C. and stirred for 15 min, followed by the addition of NH₄Cl (25 mL, sat. aq.). The crude was extracted with CH₂Cl₂ (3×25 mL), washed successively with NaHCO₃ (50 mL, sat. aq.) and brine (50 mL), dried over Na₂SO₄ and concentrated in vacuo. Aldehyde 4 was obtained as a yellow oil and used without further purification (928 mg, 93% yield).

R_(f) 0.57 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 1.18 (d, 3H, J=6.7 Hz), 3.33 (q, 1H, J=6.7 Hz), 3.57 (d, 2H, J=13.8 Hz), 3.74 (d, 2H, J=13.6 Hz), 7.23–7.42 (m, 10H), 9.73 (s, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 6.8, 54.9, 62.8, 127.3, 128.4, 128.8, 139.0, 204.5.

Exampl 2 (S)-2-(N,N-Dibenzylamino)-1-butan 1, 5

To a solution of (S)-2-amino-1-butanol (1.0 mL, 10.58 mmol) in MeOH (20 mL), BnBr (5.0 mL, 42.32 mmol) and K₂CO₃ (5.85 g, 42.32 mmol) were added. The mixture was stirred at 60° C. for 5 h, and then cooled down to room temperature and filtered, washing the solid with EtOAc. The filtrates were concentrated in vacuo and the residue purified by column chromatography on silica (100% hexane to hexane/EtOAc 5:1) to obtain alcohol 5 as a white solid (2.7 g, 95% yield).

R_(f) 0.26 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.98 (t, 3H, J=7.5 Hz), 1.25–1.37 (m, 1H), 1.79–1.89 (m, 1H), 2.74–2.83 (m, 1H), 3.31 (br s, 1H), 3.45–3.52 (m, 1H), 3.50 (d, 2H, J=13.1 Hz), 3.55–3.65 (m, 1H), 3.88 (d, 2H, J=13.3 Hz), 7.26–7.41 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 11.6, 17.8, 53.0, 60.4, 127.0, 128.3, 128.8, 139.3.

Example 3 (S)-2-(N,N-Dibenzylamino)-butyraldehyde, 6

According to the method of Example 1, from alcohol 5 (1.0 g, 3.7 mmol), aldehyde 6 was obtained as a yellow oil and used without further purification (1.0 g, 100% yield).

R_(f) 0.73 (hexane/Et₂O 1:1);

¹H NMR (300 MHz, CDCl₃) δ 0.97 (t, 3H, J=7.5 Hz), 1.64–1.85 (m, 2H), 3.08 (t, 1H, J=6.8 Hz), 3.72 (d, 2H, J=13.6 Hz), 3.80 (d, 2H, J=13.8 Hz), 7.22–7.39 (m, 10H), 9.73 (s, 1H).

Example 4 (S)-2-(N-Benzyloxycarbonylamino)-1-butanol, 7

To a cold (0° C.) solution of (S)-2-amino-1-butanol (2.0 g, 22.5 mmol) in acetone/H₂O 1:1 (50 mL), Na₂CO₃ (8.7 g, 81.9 mmol) and BnOCOCl (5.8 g, 33.8 mmol) were added. After stirring at 0° C. for 1 h, the solid was filtered off and washed with acetone (2×30 mL). The filtrates were concentrated in vacuo and the residue was purified by column chromatography on silica (100% CH₂Cl₂ to CH₂Cl₂/MeOH 20:1) to obtain alcohol 7 as a white solid (2.14 g, 43% yield).

Example 5 (S)-2-(N-Benzyloxycarbonylamino)-butyraldehyde, 8

According to the method of Example 1, from alcohol 7 (750 mg, 3.4 mmol), aldehyde 8 was obtained as a yellow oil and used without further purification (700 mg, 94% yield).

R_(f) 0.31 (MeOH/CH₂Cl₂ 3:1).

Example 6 Benzyl (S)-2-(N,N-dibenzylamino)-pentanoate, 9

To a solution of L-norvaline (685 mg, 5.85 mmol) in MeCN (15 mL), BnBr (3.48 mL, 29.24 mmol) and K₂CO₃ (4.04 g, 29.24 mmol) were added. The mixture was stirred at 60° C. for 9 h, and then cooled down to room temperature and filtered, washing the solid with EtOAc. The filtrates were concentrated in vacuo and the residue purified by column chromatography on silica (100% hexane to hexane/EtOAc 5:1) to obtain benzyl ester 9 as a colorless oil (1.6 g, 71% yield).

R_(f) 0.29 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.82 (t, 3H, J=7.4 Hz), 1.25–1.40 (m, 1H), 1.45–1.60 (m, 1H), 1.70–1.85 (m, 2H), 3.42 (dd, 1H, J=8.2, 6.7 Hz), 3.55 (d, 2H, J=13.9 Hz), 3.96 (d, 2H, J=13.9 Hz), 5.18 (d, 1H, J=12.3 Hz), 5.30 (d, 1H, J=12.3 Hz), 7.25–7.45 (m, 15H);

¹³C NMR (75 MHz, CDCl₃) δ 13.7, 19.3, 31.6, 54.4, 60.5, 65.8, 126.8, 128.1, 128.2, 128.4, 128.5, 128.8, 136.1, 139.7, 173.0.

Example 7 (S)-2-(N,N-Dibenzylamino)-1-pentanol, 10

To a cold (0° C.) suspension of LiAlH₄ (184 mg, 4.84 mmol) in THF (10 mL), a solution of ester 9 (375 mg, 0.97 mmol) in THF (2.5 mL) was added. The mixture was stirred at 0° C. for 2 h, and then quenched by dropwise addition of EtOH (3 ml). Na—K tartrate solution (10% aq, 30 mL) was added, and the crude was extracted with EtOAc (3×30 mL), dried over Na₂SO₄, concentrated in vacuo and purified by column chromatography on silica (hexane/EtOAc 5:1) to obtain alcohol 10 as a colorless oil (170 mg, 62% yield).

R_(f) 0.31 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.97 (t, 3H, J=7.1 Hz), 1.17–1.42 (m, 3H), 1.71–1.76 (m, 1H), 2.80–2.86 (m, 1H), 3.25 (br s, 1H), 3.41–3.56 (m, 2H), 3.44 (d, 2H, J=13.3 Hz), 3.85 (d, 2H, J=13.3 Hz), 7.24–7.37 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 14.3, 20.3, 27.2, 53.1, 58.7, 60.8, 127.1, 128.4, 129.0, 139.3.

Example 8 (S)-2-(N,N-Dibenzylamino)-pentanal, 11

According to the method of Example 1, from alcohol 10 (163 mg, 0.58 mmol), aldehyde 11 was obtained as a yellow oil and used without further purification (140 g, 87% yield).

R_(f) 0.73 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 0.89 (t, 3H, J=7.3 Hz), 1.34–1.44 (m, 2H), 1.60–1.76 (m, 2H), 3.17 (t, 1H, J=6.7 Hz), 3.73 (d, 2H, J=13.8 Hz), 3.81 (d, 2H, J=13.8 Hz), 7.23–7.40 (m, 10H), 9.74 (s, 1H).

Example 9 Benzyl (S)-2-(N,N-dibenzylamino)-3-methylbutyrate, 12

According to the method of Example 6, from L-valine (927 mg, 7.91 mmol), benzyl ester 12 was obtained as a colorless oil (2.58 g, 84% yield).

R_(f) 0.31 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 0.86 (d, 3H, J=6.4 Hz), 1.11 (d, 3H, J=6.5 Hz), 2.20–2.35 (m, 1H), 3.02 (d, 1H, J=10.7 Hz), 3.39 (d, 2H, J=13.9 Hz), 4.07 (d, 2H, J=13.9 Hz), 5.25 (d, 1H, J=12.3 Hz), 5.39 (d, 1H, J=12.1 Hz), 7.27–7.54 (m, 15H);

¹³C NMR (75 MHz, CDCl₃) δ 19.5, 19.9, 27.2, 54.5, 65.6, 68.0, 126.9, 128.2, 128.3, 128.5, 128.6, 128.7, 136.1, 139.4, 171.8;

ESMS calcd for C₂₆H₃₀NO₂ (M+H) 388.2, found 388.2.

Example 10 (S)-2-(N,N-Dibenzylamino)-3-methyl-1-butanol, 13

According to the method of Example 7, from ester 12 (2.3 g, 5.93 mmol), alcohol 13 was obtained as a colorless oil (1.55 g, 92% yield).

R_(f) 0.24 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 0.97 (dd, 3H, J=6.5, 1.2 Hz), 1.17 (dd, 3H, J=6.7, 1.2 Hz), 2.05–2.12 (m, 1H), 2.52–2.60 (m, 1H), 3.05 (br s, 1H), 3.47 (td, 1H, J=10.2, 1.3 Hz), 3.61 (br d, 1H, J=10.1 Hz), 3.71 (d, 2H, J=13.3 Hz), 3.91 (d, 2H, J=13.3 Hz), 7.23–7.36 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 20.1, 22.6, 27.5, 54.1, 59.1, 64.6, 127.1, 128.4, 129.1, 139.6;

ESMS calcd for C₁₉H₂₆NO (M+H) 284.2, found 284.2.

Example 11 (S)-2-(N,N-Dibenzylamino)-3-methylbutyraldehyde, 14

According to the method of Example 1, from alcohol 13 (450 mg, 1.59 mmol), aldehyde 14 was obtained as a yellow oil and used without further purification (447 mg, 100% yield).

R_(f) 0.57 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (d, 3H, J=6.5 Hz), 1.08 (d, 3H, J=6.5 Hz), 2.25–2.32 (m, 1H), 2.72 (dd, 1H, J=10.2, 3.7 Hz), 3.70 (d, 2H, J=13.6 Hz), 4.02 (d, 2H, J=13.8 Hz), 7.24–7.38 (m, 10H), 9.85 (d, 1H, J=3.5 Hz).

Example 12 Benzyl (2S,3S)-2-(N,N-dibenzylamino)-3-methylpentanoate, 15

According to the method of Example 6, from L-isoleucine (1.0 g, 7.6 mmol), benzyl ester 15 was obtained as a colorless oil (2.4 g, 80% yield).

R_(f) 0.62 (hexane/EtOAc 20:1);

¹H NMR (300 MHz, CDCl₃) δ 0.71–0.79 (m, 6H), 1.09–1.21 (m, 1H), 1.82–2.01 (m, 2H), 3.02 (d, 1H, J=6.5 Hz), 3.23 (d, 2H, J=9.5 Hz), 3.89 (d, 2H, J=9.5 Hz), 5.15 (d, 1H, J=7.5 Hz), 5.24 (d, 1H, J=7.5 Hz), 7.11–7.46 (m, 15H);

ESMS calcd for C₂₇H₃₂NO₂ (M+H) 402.2, found 402.5.

Example 13 (2S,3S)-2-(N,N-Dibenzylamino)-3-methyl-1-pentanol, 16

According to the method of Example 7, from ester 15 (0.50 g, 1.23 mmol), alcohol 16 was obtained as a colorless oil (0.36 g, 99% yield).

R_(f) 0.43 (hexane/EtOAc 9:1);

¹H NMR (300 MHz, CDCl₃) δ 0.92–0.99 (m, 6H), 1.13–1.18 (m, 1H), 1.63–1.67 (m, 1H), 1.88–1.97 (m, 1H), 2.63–2.67 (m, 1H), 3.45 (d, 2H, J=6.5 Hz), 3.49 (d, 2H, J=9.5 Hz), 3.88 (d, 2H, J=9.5 Hz), 7.18–7.42 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 11.4, 15.8, 28.2, 32.7, 53.9, 58.7, 62.7, 127.0, 128.3, 129.0, 139.7;

ESMS calcd for C₂₀H₂₈NO (M+H) 298.4, found 298.4.

Example 14 (2S,3S)-2-(N,N-Dibenzylamino)-3-methylpentanal, 17

According to the method of Example 1, from alcohol 16 (479 mg, 1.61 mmol), aldehyde 17 was obtained as a yellow oil and used without further purification (470 mg, 98% yield).

R_(f) 0.71 (hexane/EtOAc 9:1);

¹H NMR (300 MHz, CD₃OD) δ 0.78–0.82 (m, 6H), 1.13–1.20 (m, 1H), 1.80–1.85 (m, 1H), 2.02–2.10 (m, 1H), 2.71 (dd, 1H, J=7.8, 3.5 Hz), 3.61 (d, 2H, J=11.8 Hz), 3.99 (d, 2H, J=11.8 Hz), 7.15–7.29 (m, 10H), 9.77 (d, 1H, J=2.0 Hz).

Example 15 Benzyl (S)-3-(4′-benzyloxyphenyl)-2-(N,N-dibenzylamino)-propionate, 18

According to the method of Example 6, from L-tyrosine (1.49 g, 8.22 mmol), ester 18 was obtained as a colorless oil (2.10 g, 47% yield).

R_(f) 0.25 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 3.06 (dd, 1H, J=14.0, 8.1 Hz), 3.20 (dd, 1H, J=14.0, 7.6 Hz), 3.65 (d, 2H, J=13.9 Hz), 3.79 (t, 1H, J=7.7 Hz), 4.04 (d, 2H, J=13.9 Hz), 5.15 (s, 2H), 5.22 (d, 1H, J=12.2 Hz), 5.33 (d, 1H, J=12.2 Hz), 6.94 (d, 2H, J=8.8 Hz), 7.03 (d, 2H, J=8.5 Hz), 7.26–7.57 (m, 20H);

¹³C NMR (75 MHz, CDCl₃) δ 34.7, 54.3, 62.5, 65.9, 69.9, 102.1, 114.5, 126.8, 127.4, 127.8, 128.1, 128.2, 128.4, 128.5, 128.5, 128.6, 130.3, 135.9, 137.1, 139.2, 157.3, 172.1;

ESMS calcd for C₃₇H₃₆NO₃ (M+H) 542.3, found 542.3.

Example 16 (S)-3-(4′-Benzyloxyphenyl)-2-(N,N-dibenzylamino)-1-propanol, 19

According to the method of Example 7, from ester 18 (1.90 g, 3.51 mmol), alcohol 19 was obtained as a colorless oil (1.20 g, 78% yield).

R_(f) 0.15 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 2.45 (dd, 1H, J=14.6, 10.7 Hz), 3.05–3.15 (m, 3H), 3.44 (br s, 1H), 3.52–3.60 (m, 1H), 3.55 (d, 2H, J=13.3 Hz), 3.98 (d, 2H, J=13.3 Hz), 5.10 (s, 2H), 6.97 (d, 2H, J=8.6 Hz), 7.08 (d, 2H, J=8.4 Hz), 7.29–7.52 (m, 15H);

¹³C NMR (75 MHz, CDCl₃) δ 30.8, 53.1, 60.3, 60.8, 69.9, 114.9, 127.2, 127.3, 127.8, 128.4, 128.5, 128.9, 129.8, 131.3, 137.0, 139.1, 157.2;

ESMS calcd for C₃₀H₃₂NO₂ (M+H) 438.2, found 438.3.

Example 17 (S)-2-(N,N-dibenzylamino)-3-(4′-benzyloxyphenyl)-propionaldehyde, 20

According to the method of Example 1, from alcohol 19 (600 mg, 1.37 mmol), aldehyde 20 was obtained as a yellow oil and used without further purification (597 mg, 100% yield).

R_(f) 0.38 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 2.89 (dd, 1H, J=14.1, 6.1 Hz), 3.09 (dd, 1H, J=14.1, 7.2 Hz), 3.51 (t, 1H, J=6.8 Hz), 3.67 (d, 2H, J=13.8 Hz), 3.82 (d, 2H, J=13.8 Hz), 5.06 (s, 2H), 6.88 (d, 2H, J=8.7 Hz), 7.06 (d, 2H, J=8.6 Hz), 7.22–7.45 (m, 15H), 9.72 (s, 1H).

Example 18 Methyl (S)-2,5-bis-(N,N-dibenzylamin)-pentanoate, 21

According to the method of Example 6, from L-ornitine methyl ester (1.20 g, 5.48 mmol), ester 21 was obtained as a colorless oil (2.18 g, 79% yield).

R_(f) 0.27 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 1.50–1.60 (m, 1H), 1.75–1.90 (m, 3H), 2.41 (t, 2H, J=6.7 Hz), 3.36 (t, 1H, J=7.3 Hz), 3.55 (d, 2H, J=13.8 Hz), 3.63 (d, 2H, J=13.9 Hz), 3.65 (d, 2H, J=13.6 Hz), 3.84 (s, 3H), 4.02 (d, 2H, J=13.8 Hz), 7.29–7.45 (m, 20H);

¹³C NMR (75 MHz, CDCl₃) δ 23.6, 27.2, 50.8, 52.9, 54.5, 58.2, 60.6, 126.7, 126.9, 128.0, 128.1, 128.7, 128.8, 139.6, 139.7, 173.4;

ESMS calcd for C₃₄H₃₉N₂O₂ (M+H) 507.3, found 507.3.

Example 19 (S)-2,5-Bis-(N,N-dibenzylamino)-1-pentanol, 22

According to the method of Example 7, from ester 21 (1.75 g, 3.45 mmol), alcohol 22 was obtained as a colorless oil (1.50 g, 91% yield).

R_(f) 0.27 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 1.25–1.35 (m, 1H), 1.53–1.63 (m, 2H), 1.78–1.89 (m, 1H), 2.60 (t, 2H, J=6.8 Hz), 2.83–2.93 (m, 1H), 3.35 (br s, 1H), 3.53 (d, 2H, J=13.3 Hz), 3.54–3.64 (m, 2H), 3.70 (d, 2H, J=13.6 Hz), 3.76 (d, 2H, J=13.8 Hz), 3.93 (d, 2H, J=13.3 Hz), 7.36–7.59 (m, 20H);

¹³C NMR (75 MHz, CDCl₃) δ 22.7, 24.6, 53.0, 53.6, 58.4, 58.9, 60.7, 126.7, 127.0, 128.0, 128.2, 128.6, 128.8, 139.2, 139.6;

ESMS calcd for C₃₃H₃₉N₂O (M+H) 479.3, found 479.3.

Example 20 (S)-2,5-Bis-(N,N-dibenzylamino)-pentanal, 23

According to the method of Example 1, from alcohol 22 (505 mg, 1.05 mmol), aldehyde 23 was obtained as a yellow oil and used without further purification (503 mg, 100% yield).

R_(f) 0.57 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 1.30–1.40 (m, 1H), 1.55–1.70 (m, 2H), 1.75–1.85 (m, 1H), 2.35–2.45 (m, 2H), 3.02–3.08 (m, 1H), 3.52 (d, 2H, J=13.6 Hz), 3.62 (d, 2H, J=13.6 Hz), 3.71 (d, 2H, J=13.8 Hz), 3.81 (d, 2H, J=13.8 Hz), 7.28–7.41 (m, 20H), 9.69 (s, 1H).

Example 21 Methyl (R)-2-(N,N-dibenzylamino)-propionate, 24

According to the method of Example 6, from D-alanine methyl ester (536 mg, 3.84 mmol), ester 24 was obtained as a colorless oil (625 mg, 57% yield).

R_(f) 0.40 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 1.35 (d, 3H, J=7.1 Hz), 3.53 (q, 1H, J=7.0 Hz), 3.65 (d, 2H, J=13.8 Hz), 3.75 (s, 3H), 3.85 (d, 2H, J=13.8 Hz), 7.22–7.42 (m, 10H).

Example 22 (R)-2-(N,N-dibenzylamino)-1-propanol, 25

According to the method of Example 7, from ester 24 (625 mg, 2.20 mmol), alcohol 25 was obtained as a colorless oil (450 mg, 80% yield).

R_(f) 0.21 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.98 (d, 3H, J=7.1 Hz), 2.95–3.05 (m, 1H), 3.13 (br s, 1H), 3.35 (d, 2H, J=13.8 Hz), 3.40–3.55 (m, 2H), 3.81 (d, 2H, J=13.8 Hz), 7.19–7.41 (m, 10H).

Example 23 (R)-2-(N,N-Dibenzylamino)-propionaldehyde, 26

According to the method of Example 1, from alcohol 25 (475 mg, 1.86 mmol), aldehyde 26 was obtained as a yellow oil and used without farther purification (445 mg, 94% yield).

R_(f) 0.5⁷ (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 1.18 (t, 3H, J=6.7 Hz), 3.33 (q, 1H, J=6.7 Hz), 3.57 (d, 2H, J=13.8 Hz), 3.74 (d, 2H, J=13.6 Hz), 7.23–7.42 (m, 10H), 9.73 (s, 1H).

Example 24 (S)-2Benzyloxycarbonylamino)-1-propanol, 27

To a cold (−15° C.) solution of N-Cbz-L-alanine (1.0 g, 4.5 mmol) in THF (15 mL), Et₃N (360 mg, 4.5 mmol) and i-BuOCOCl (610 mg, 4.5 mmol) were added. After stirring at room temperature for 20 min, the solid Et₃N.HCl was filtered off and washed with THF. The filtrates were cooled to −15° C. and a solution of NaBH₄ (260 mg, 6.75 mmol) in H₂O (10 mL) was added. After 1 h, the reaction was quenched with H₂O (70 mL) and the THF removed in vacuo. The residue was extracted with EtOAc (3×30 mL), washed with brine (100 mL), dried over MgSO₄ and concentrated in vacuo to obtain alcohol 27 as a white solid (780 mg, 82% yield).

¹H NMR (500 MHz, CDCl₃) δ 1.15 (d, 3H, J=6.8 Hz), 2.75–2.80 (m, 2H), 3.45–3.55 (m, 1H), 3.60–3.65 (m, 1H), 3.80–3.85 (m, 1H), 5.09 (s, 2H), 7.30–7.35 (m, 5H).

Example 25 (S)-2-(N-Benzyloxycarbonylamino)-propionaldehyde, 28

According to the method of Example 1, from alcohol 27 (750 mg, 3.6 mmol), aldehyde 28 was obtained as a yellow oil and used without further purification (680 mg, 92% yield).

R_(f) 0.31 (MeOH/CH₂Cl₂ 3:1).

Example 26 (2S,3R)-2-(N,N-Dibenzylamino)-3-tetradecanol, 29

To a suspension of Mg (155 mg, 6.38 mmol) and a few crystals of I₂ in THF (3.1 mL), an aliquot of 1-bromoundecane (0.25 mL, 1.12 mmol) was added and the mixture was stirred at 60° C. until the red color of the solution disappeared. Then the remainder of 1-bromoundecane (0.46 mL, 2.07 mmol) was added and the reaction was stirred at room temperature for 1 h. The Grignard solution formed thereof was cooled down to 0° C. and a solution of aldehyde 4 (323.5 mg, 1.28 mmol) in THF (1.6 mL) was added via cannula. After stirring overnight at room temperature, the reaction was quenched with HCl (3N, 10 mL) extracted with EtOAc (3×10 mL), washed successively with NaHCO₃ (20 mL, sat. aq.) and brine (20 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (100% hexane to 10:1 hexane/EtOAc) to obtain a mixture of diastereoisomers. Further purification by HPLC on silica (95:5 to 80:20 hexane/MTBE) afforded pure anti alcohol 29 as a colorless oil (205 mg, 39% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.92 (t, 3H, J=6.9 Hz), 1.13 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 18H), 1.65–1.80 (m, 2H), 1.87 (br s, 1H), 2.74 (quint, 1H, J=6.7 Hz), 3.49 (d, 2H, J=13.9 Hz), 3.57–3.65 (m, 1H), 3.79 (d, 2H, J=13.8 Hz), 7.22–7.38 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.6, 29.6, 29.7, 31.9, 34.3, 54.8, 57.3, 73.7, 126.9, 128.2, 128.8, 140.2;

ESMS calcd for C₂₈H₄₄NO (M+H) 410.3, found 410.6.

Example 27 (2S,3R)-2-Amino-3-tetradecanol, 30

To a solution of N,N-dibenzylamine 29 (182 mg, 0.44 mmol) in MeOH (4.5 mL) at room temperature, Pd(OH)₂—C (20% wt, 24 mg, 0.04 mmol) was added. The mixture was purged with a stream of dry Ar, and then H₂. The reaction was stirred overnight under a H₂ atmosphere (1 atm). The catalyst was filtered off through a 0.45 μm teflon filter in polypropylene housing, washing the filter with MeOH (30 mL) and the solvent was evaporated in vacuo. The crude was purified by column chromatography on silica (90:10 CH₂Cl₂/MeOH to 100% MeOH) to obtain aminoalcohol 30 as a white solid (87 mg, 85% yield).

¹H NMR (300 MHz, CDCl₃) □ 0.87 (t, 3H, J=6.7 Hz), 1.03 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 18H), 1.45–1.55 (m, 2H), 2.66 (br s, 3H), 2.95–3.05 (m, 1H), 3.45–3.55 (m, 1H); ¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.2, 22.7, 26.2, 29.3, 29.6, 29.8, 31.9, 32.5, 50.5, 74.2;

ESMS calcd for C₁₄H₃₂NO (M+H) 230.2, found 230.4.

Example 28 (2S,3R)-2-(N,N-Dibenzylamino)-3-pentadecanol, 31

According to the method of Example 26, from aldehyde 4 (273 mg, 1.08 mmol) and 1-bromododecane (671 mg, 2.69 mmol), alcohol 31 was obtained as a colorless oil (195 mg, 43% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.90 (t, 3H, J=6.9 Hz), 1.12 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 20H), 1.65–1.75 (m, 2H), 1.82 (br s, 1H), 2.73 (quint, 1H, J=6.7 Hz), 3.48 (d, 2H, J=13.8 Hz), 3.57–3.65 (m, 1H), 3.78 (d, 2H, J=13.8 Hz), 7.21–7.37 (m, 10H); ¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.6, 29.6, 29.7, 31.9, 34.3, 54.8, 57.3, 73.7, 126.9, 128.2, 128.8, 140.2;

ESMS calcd for C₂₉H₄₆NO (M+H) 424.4, found 424.7.

Example 29 (2S,3R)-2-Amino-3-pentadecanol, 32

According to the method of Example 27, from N,N-dibenzylamine 31 (145 mg, 0.34 mmol), aminoalcohol 32 was obtained as a white solid (65 mg, 78% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.9 Hz), 1.02 (d, 3H, J=6.4 Hz), 1.20–1.40 (m, 20H), 1.45–1.55 (m, 2H), 2.38 (br s, 3H), 2.93–3.03 (m, 1H), 3.42–3.52 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.4, 22.7, 26.2, 29.3, 29.6, 29.8, 31.9, 32.5, 50.5, 74.4;

ESMS calcd for C₁₅H₃₄NO (M+H) 244.3, found 244.4.

Example 30 (2S,3R)-2-(N,N-Dibenzylamino)-3-hexadecanol, 33

According to the method of Example 26, from aldehyde 4 (332 mg, 1.31 mmol) and 1-bromotridecane (863 mg, 3.28 mmol), alcohol 33 was obtained as a colorless oil (172 mg, 30% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.90 (t, 3H, J=6.9 Hz), 1.12 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 22H), 1.65–1.75 (m, 2H), 1.84 (br s, 1H), 2.73 (quint, 1H, J=6.5 Hz), 3.49 (d, 2H, J=13.8 Hz), 3.57–3.65 (m, 1H), 3.78 (d, 2H, J=13.8 Hz), 7.23–7.38 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.6, 29.7, 31.9, 34.3, 54.8, 57.3, 73.6, 126.8, 128.2, 128.7, 140.2;

ESMS calcd for C₃₀H₄₈NO (M+H) 438.4, found 438.7.

Example 31 (2S,3R)-2-Amino-3-hexadecanol, 34

According to the method of Example 27, from N,N-dibenzylamine 33 (149 mg, 0.34 mmol), aminoalcohol 34 was obtained as a white solid (62 mg, 71% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=7.0 Hz), 1.05 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 22H), 1.45–1.55 (m, 2H), 2.95–3.10 (m, 4H), 3.48–3.58 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 15.9, 22.7, 26.2, 29.3, 29.6, 29.7, 29.7, 31.9, 32.6, 50.6, 73.9;

ESMS calcd for C₁₆H₃₆NO (M+H) 258.3, found 258.5.

Example 32 (2S,3R)-2-Amino-3-hexadecanol hydrochloride, 35

To a solution of amine 34 (26 mg, 0.10 mmol) in dioxane (0.5 mL), anhydrous HCl solution in dioxane (5.3M, 0.38 mL, 2.02 mmol) was added. After stirring at room temperature for 5 h, the solvent was removed in vacuo. The resulting solid was washed with dioxane to obtain hydrochloride 35 as a white solid (19 mg, 64% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.7 Hz), 1.21 (d, 3H, J=6.7 Hz), 1.25–1.40 (m, 22H), 1.45–1.60 (m, 2H), 3.27 (qd, 1H, J=6.7, 3.0 Hz), 3.65–3.73 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 12.1, 14.4, 23.7, 27.0, 30.5, 30.6, 30.7, 30.7, 30.8, 33.1, 34.0, 52.6, 71.6;

ESMS calcd for C₁₆H₃₆NO (M−Cl) 258.3, found 258.4.

Example 33 (2S,3R)-2-(N,N-Dibenzylamino)-3-heptadecanol, 36

According to the method of Example 26, from aldehyde 4 (309 mg, 1.21 mmol) and 1-bromotetradecane (1.34 g, 4.84 mmol), alcohol 36 was obtained as a colorless oil (270 mg, 49% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.91 (t, 3H, V 6.9 Hz), 1.12 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 24H), 1.65–1.75 (m, 2H), 1.85 (br s, 1H), 2.73 (quint, 1H, J=7 6.4 Hz), 3.49 (d, 2H, J=13.9 Hz), 3.57–3.65 (m, 1H), 3.78 (d, 2H, J=13.8 Hz), 7.21–7.38 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.6, 29.7, 31.9, 34.4, 54.8, 57.3, 73.6, 126.9, 128.2, 128.8, 140.2;

ESMS calcd for C₃₁H₅₀NO (M+H) 452.4, found 452.5.

Example 34 (2S,3R)-2-Amino-3-heptadecanol, 37

According to the method of Example 27, from N,N-dibenzylamine 36 (182 mg, 0.40 mmol), aminoalcohol 37 was obtained as a white solid (81 mg, 74% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=7.0 Hz), 1.02 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 24H), 1.45–1.55 (m, 2H), 1.85 (br s, 3H), 2.94–3.04 (m, 1H), 3.42–3.52 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.3, 22.7, 26.2, 29.3, 29.7, 31.9, 32.5, 50.4, 74.2;

ESMS calcd for C₁₇H₃₈NO (M+H) 272.3, found 272.3.

Example 35 (2S,3R)-2-Amino-3-heptadecanol hydrochloride, 38

According to the method of Example 32, from aminoalcohol 37 (50 mg, 0.18 mmol), hydrochloride 38 was obtained as a white solid (41 mg, 73% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.80 (t, 3H, J=6.8 Hz), 1.22 (d, 3H, J=6.8 Hz), 1.21–1.40 (m, 24H), 1.41–1.51 (m, 2H), 3.22–3.31 (m, 1H), 3.63–3.74 (m, 1H).

Example 36 Bis-((2S,3R)-2-ammonium-3-octadecanol) L-tartrate, 40

To a solution of aminoalcohol 1 (63 mg, 0.221 mmol) in MeOH (1.1 mL) at room temperature, L-tartaric acid (66 mg, 0.442 mmol) was added. After stirring for 16 h, the solvent was evaporated in vacuo. The resulting solid was washed with H₂O and dried under vacuum for 8 h to obtain tartrate 40 as a white solid (53 mg, 67% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.7 Hz), 1.21 (d, 3H, J=6.7 Hz), 1.25–1.40 (m, 26H), 1.40–1.55 (m, 2H), 3.26 (qd, 1H, J=6.7, 3.0 Hz), 3.62–3.72 (m, 1H), 4.43 (d, 2H, J=1.8 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 12.0, 14.4, 23.7, 27.0, 30.5, 30.8, 33.1, 34.0, 52.6, 71.7, 73.9;

ESMS calc for C₁₈H₄₀NO (M=CHOHCO₂) 286.3, found 286.2.

Example 37 (2S,3R)-2-Amino-3-octadecanol hydrochloride, 41

According to the method of Example 32, from aminoalcohol 1 (52.5 mg, 0.184 mmol), hydrochloride 41 was obtained as a white solid (52 mg, 88% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.7 Hz), 1.21 (d, 3H, J=6.7 Hz), 1.25–1.40 (m, 26H), 1.40–1.55 (m, 2H), 3.26 (qd, 1H, J=6.7, 3.0 Hz), 3.62–3.72 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 12.1, 14.5, 23.7, 27.0, 30.5, 30.7, 30.7, 30.8, 33.1, 34.0, 52.6, 71.6;

ESMS calcd for C₁₈H₄₀NO (M−Cl) 286.3, found 286.2.

Example 38 (2S,3R)-2-(N,N-Dibenzylamino)-3-nonadecanol, 42

According to the method of Example 26, from aldehyde 4 (294 mg, 1.16 mmol) and 1-bromohexadecane (1.42 g, 4.64 mmol), alcohol 42 was obtained as a colorless oil (283 mg, 51% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.93 (t, 3H, J=6.9 Hz), 1.14 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 28H), 1.65–1.80 (m, 2H), 1.95 (br s, 1H), 2.75 (quint, 1H, J=6.5 Hz), 3.50 (d, 2H, J=13.8 Hz), 3.57–3.65 (m, 1H), 3.80 (d, 2H, J=13.8 Hz), 7.23–7.40 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.6, 29.7, 31.9, 34.3, 54.7, 57.2, 73.6, 126.8, 128.2, 128.7, 140.1;

ESMS calcd for C₃₃H₅₄NO (M+H) 480.4, found 480.5.

Example 39 (2S,3R)-2-Amino-3-nonadecanol, 2

According to the method of Example 27, from N,N-dibenzylamine 42 (204 mg, 0.43 mmol), aminoalcohol 2 was obtained as a white solid (91 mg, 72% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=6.9 Hz), 1.01 (d, 3H, J=6.4 Hz), 1.20–1.40 (m, 28H), 1.45–1.55 (m, 2H), 1.77 (br s, 3H), 2.92–3.02 (m, 1H), 3.39–3.49 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.7, 22.7, 26.2, 29.3, 29.6, 29.7, 29.8, 31.9, 32.4, 50.3, 74.6;

ESMS calcd for C₁₉H₄₂NO (M+H) 300.3, found 300.3.

Example 40 (2S,3R)-2-Amino-3-nonadecanol hydrochloride, 43

According to the method of Example 32, from aminoalcohol 2 (530 mg, 1.70 mmol), hydrochloride 43 was obtained as a white solid (454 mg, 76% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.86 (t, 3H, J=6.8 Hz), 1.35 (d, 3H, J=6.8 Hz), 1.20–1.41 (m, 28H), 1.41–1.51 (m, 2H), 3.24–3.37 (m, 1H), 3.65–3.73 (m, 1H).

Example 41 (2S,3R)-2-(N,N-Dibenzylamino)-3-eicosanol, 44

According to the method of Example 26, from aldehyde 4 (410 mg, 1.62 mmol) and 1-bromoheptadecane (2.07 g, 6.47 mmol), alcohol 44 was obtained as a colorless oil (427 mg, 53% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.93 (t, 3H, J=6.9 Hz), 1.14 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 30H), 1.65–1.80 (m, 2H), 1.94 (br s, 1H), 2.75 (quint, 1H, J=6.7 Hz), 3.51 (d, 2H, J=13.8 Hz), 3.56–3.64 (m, 1H), 3.80 (d, 2H, J=13.8 Hz), 7.23–7.40 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.6, 29.6, 29.7, 31.9, 34.3, 54.8, 57.3, 73.6, 126.8, 128.2, 128.7, 140.2;

ESMS calcd for C₃₄H₅₆NO (M+H) 494.4, found 494.5.

Example 42 (2S,3R)-2-Amino-3-eicosanol, 3

According to the method of Example 27, from N,N-dibenzylamine 44 (294 mg, 0.60 mmol), aminoalcohol 3 was obtained as a white solid (140 mg, 75% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=6.7 Hz), 1.00 (d, 3H, J=6.4 Hz), 1.20–1.40 (m, 30H), 1.45–1.55 (m, 2H), 1.70 (br s, 3H), 2.92–3.02 (m, 1H), 3.39–3.49 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.8, 22.7, 26.2, 29.3, 29.7, 29.8, 31.9, 32.5, 50.4, 74.7;

ESMS calcd for C₂₀H₄₄NO (M+H) 314.3, found 314.3.

Example 43 (2S,3R)-2-Amino-3-eicosanol hydrochloride, 45

According to the method of Example 32, from aminoalcohol 3 (12 mg, 0.04 mmol), hydrochloride 45 was obtained as a white solid (11 mg, 82% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.5 Hz), 1.21 (d, 3H, J=6.7 Hz), 1.25–1.40 (m, 30H), 1.45–1.60 (m, 2H), 3.26 (qd, 1H, J=6.9, 3.0 Hz), 3.63–3.73 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 12.1, 14.4, 23.7, 27.8, 30.5, 30.6, 30.8, 33.1, 34.0, 52.6, 71.7;

ESMS calcd for C₂₀H₄₄NO (M−Cl) 314.3, found 314.5.

Example 44 (2S,3R)-2-(N,N-Dibenzylamino)-3-heneicosanol, 46

According to the method of Example 26, from aldehyde 4 (350 mg, 1.38 mmol) and 1-bromooctadecane (1.15 g, 3.45 mmol), alcohol 46 was obtained as a colorless oil (395 mg, 56% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.91 (t, 3H, J=6.9 Hz), 1.14 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 32H), 1.65–1.75 (m, 2H), 1.80 (br s, 1H), 2.75 (quint, 1H, J=6.7 Hz), 3.51 (d, 2H, J=13.9 Hz), 3.56–3.64 (m, 1H), 3.80 (d, 2H, J=13.8 Hz), 7.23–7.40 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.7, 31.9, 34.3, 54.8, 57.2, 73.6, 126.8, 128.2, 128.7, 140.1;

ESMS calcd for C₃₅H₅₈NO (M+H) 508.4, found 508.4.

Example 45 (2S,3R)-2-Amino-3-heneicosanol, 47

According to the method of Example 27, from N,N-dibenzylamine 46 (228 mg, 0.45 mmol), aminoalcohol 47 was obtained as a white solid (125 mg, 85% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J7 6.9 Hz), 1.00 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 32H), 1.45–1.55 (m, 2H), 1.86 (br s, 3H), 2.92–3.02 (m, 1H), 3.39–3.49 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.8, 22.7, 26.2, 29.3, 29.7, 29.8, 31.9, 32.5, 50.4, 74.7;

ESMS calcd for C₂₁H₄₆NO (M+H) 328.3, found 328.3.

Example 46 (2S,3R)-2-Amino-3-heneicosanol hydrochloride, 48

According to the method of Example 32, from aminoalcohol 47 (32.5 mg, 0.10 mmol), hydrochloride 48 was obtained as a white solid (32 mg, 89% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.6 Hz), 1.21 (d, 3H, J=6.9 Hz), 1.25–1.40 (m, 32H), 1.45–1.60 (m, 2H), 3.27 (qd, 1H, J=6.9, 3.0 Hz), 3.65–3.73 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 12.1, 14.5, 23.8, 27.0, 30.5, 30.7, 30.7, 30.8, 33.1, 34.0, 52.6, 71.6;

ESMS calcd for C₂₁H₄₆NO (M−Cl) 328.3, found 328.5.

Example 47 (2S,3R)-2-(N,N-Dibenzylamino)-3-docosanol, 49

According to the method of Example 26, from aldehyde 4 (380 mg, 1.50 mmol) and 1-bromononadecane (1.30 g, 3.75 mmol), alcohol 49 was obtained as a colorless oil (349 mg, 45% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.91 (t, 3H, J=6.9 Hz), 1.14 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 34H), 1.65–1.75 (m, 2H), 1.81 (br s, 1H), 2.75 (quint, 1H, J=6.7 Hz), 3.51 (d, 2H, J=13.9 Hz), 3.56–3.64 (m, 1H), 3.80 (d, 2H, J=13.8 Hz), 7.23–7.40 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.7, 31.9, 34.3, 54.8, 57.2, 73.6, 126.8, 128.2, 128.7, 140.1;

ESMS calcd for C₃₆H₆₀NO (M+H) 522.5, found 522.4.

Example 48 (2S,3R)-2-Amino-3-docosanol, 50

According to the method of Example 27, from N,N-dibenzylamine 49 (206 mg, 0.39 mmol), aminoalcohol 50 was obtained as a white solid (100 mg, 74% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.9 Hz), 1.00 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 34H), 1.45–1.55 (m, 2H), 1.65 (br s, 3H), 2.92–3.02 (m, 1H), 3.39–3.49 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.8, 22.7, 26.2, 29.3, 29.7, 29.8, 31.9, 32.5, 50.4, 74.7;

ESMS calcd for C₂₂H₄₈NO (M+H) 342.4, found 342.4.

Example 49 (2S,3R)-2-(N,N-Dibenzylamino)-3-tricosanol, 51

According to the method of Example 26, from aldehyde 4 (365 mg, 1.44 mmol) and 1-bromoeicosadecane (1.30 g, 3.60 mmol), alcohol 51 was obtained as a colorless oil (317 mg, 41% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.91 (t, 3H, J=6.9 Hz), 1.14 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 36H), 1.65–1.75 (m, 2H), 1.81 (br s, 1H), 2.75 (quint, 1H, J=6.7 Hz), 3.51 (d, 2H, J=13.9 Hz), 3.56–3.64 (m, 1H), 3.80 (d, 2H, J=13.8 Hz), 7.23–7.40 (m, 10H);

¹⁴C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.6, 25.8, 9.3, 29.7, 31.9, 34.3, 54.7, 57.2, 73.6, 126.8, 128.2, 128.7, 140.1;

ESMS calcd for C₃₇H₆₂NO (M+H) 536.5, found 536.5.

Example 50 (2S,3R)-2-Amino-3-tricosanol, 52

According to the method of Example 27, from N,N-dibenzylamine 51 (191 mg, 0.36 mmol), aminoalcohol 52 was obtained as a white solid (103 mg, 81% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.9 Hz), 1.00 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 36H), 1.45–1.55 (m, 2H), 1.65 (br s, 3H), 2.92–3.02 (m, 1H), 3.39–3.49 (m, 1H);

¹³C NMR (75 MHz, CDCl₁) δ 14.1, 16.8, 22.7, 26.2, 29.3, 29.7, 29.8, 31.9, 32.5, 50.4, 74.7;

ESMS calcd for C₂₃H₅₀NO (M+H) 356.4, found 356.4.

Example 51 (3S,4R)-3-(N,N-Dibenzylamino)4octadecanol, 53

According to the method of Example 26, from aldehyde 6 (660 mg, 2.47 mmol) and 1-bromotetradecane (1.71 g, 6.17 mmol), alcohol 53 was obtained as a colorless oil (535 mg, 47% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.92 (t, 3H, J=6.6 Hz), 1.02 (t, 3H, J=7.4 Hz), 1.20–1.40 (m, 24H), 1.45–1.60 (m, 3H), 1.70–1.85 (m, 1H), 2.27 (br s, 1H), 2.62 (td, 1H, J=7.0, 4.2 Hz), 3.60–3.75 (m, 5H), 7.22–7.38 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 12.3, 14.1, 18.1, 22.7, 26.6, 29.4, 29.6, 29.7, 31.9, 34.4, 55.2, 62.8, 70.6, 126.9, 128.2, 128.9, 140.1;

ESMS calcd for C₃₂H₅₂NO (M+H) 466.4, found 466.4.

Example 52 (3S,4R)-3-Amino-4-octadecanol, 54

According to the method of Example 27, from N,N-dibenzylamine 53 (166 mg, 0.36 mmol), aminoalcohol 54 was obtained as a white solid (100 mg, 98% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.89 (t, 3H, J=6.6 Hz), 1.00 (t, 3H, J=7.5 Hz), 1.20–1.40 (m, 26H), 1.45–1.60 (m, 2H), 2.05 (br s, 3H), 2.64–2.70 (m, 1H), 3.42–3.50 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 11.0, 14.1, 22.7, 24.8, 26.2, 29.3, 29.6, 29.7, 29.8, 31.5, 31.9, 57.1, 74.0;

ESMS calcd for C₁₈H₄₀NO (M+H) 286.3, found 286.2.

Example 53 (3s,4R)-3-Amino-4-octadecanol hydrocloride, 55

According to the method of Example 32, from aminoalcohol 54 (52 mg, 0.18 mmol), hydrochloride 55 was obtained as a white solid (38 mg, 65% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.7 Hz), 1.04 (t, 3H, J=7.4 Hz), 1.25–1.50 (m, 26H), 1.55–1.80 (m, 2H), 3.04–3.12 (m, 1H), 3.70–3.80 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 10.6, 14.5, 21.4, 23.8, 27.1, 30.5, 30.6, 30.7, 30.8, 33.0, 33.1, 59.0, 71.4;

ESMS calcd for C₁₈H₄₀NO (M−Cl) 286.3, found 286.2.

Example 54 (3S,4R)-3-(N,N-Dibenzylamino)-4-nonadecanol, 56

According to the method of Example 26, from aldehyde 6 (1.0 g, 3.7 mmol) and 1-bromopentadecane (6.55 g, 22.5 mmol), alcohol 56 was obtained as a colorless oil (800 mg, 45% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=6.8 Hz), 0.99 (t, 3H, J=7.4 Hz), 1.20–1.35 (m, 26H), 1.40–1.55 (m, 3H), 1.70–1.80 (m, 1H), 2.56–2.62 (m, 1H), 3.60–3.75 (m, 5H), 7.26–7.46 (m, 10H).

Example 55 (3S,4R)-3-Amino-4-nonadecanol, 57

According to the method of Example 27, from N,N-dibenzylamine 56 (400 mg, 0.83 mmol), aminoalcohol 57 was obtained as a white solid (220 mg, 88% yield).

¹H NMR (500, MHz, CD₃OD) δ 0.80 (t, 3H, J=7.1 Hz), 0.91 (t, 3H, J=7.5 Hz), 1.15–1.25 (m, 26H), 1.30–1.40 (m, 2H), 1.40–1.50 (m, 1H), 1.55–1.65 (m, 1H), 2.70–2.75 (m, 1H), 3.45–3.50 (m, 1H);

¹³C NMR (125 MHz, CD₃OD) δ 11.8, 15.4, 24.5, 24.7, 28.1, 31.4, 31.7, 33.9, 34.0, 59.8, 74.3;

ESMS calcd for C₁₉H₄₂NO (M+H) 300.3, found 300.4.

Example 56 (3S,4R)-3-Amino-4-nonadecanol hydrochloride, 58

According to the method of Example 32, from aminoalcohol 57 (20 mg, 0.07 mmol), hydrochloride 58 was obtained as a white solid (6 mg, 27% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.6 Hz), 1.04 (t, 3H, J=7.6 Hz), 1.25–1.50 (m, 28H), 1.55–1.80 (m, 2H), 3.04–3.12 (m, 1H), 3.70–3.80 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 10.6, 14.4, 21.4, 23.8, 27.1, 30.5, 30.6, 30.8, 33.0, 33.1, 59.0, 71.4;

ESMS calcd for C₁₉H₄₂NO (M−Cl) 300.3, found 300.5.

Example 57 (3S,4R)-3-(N,N-Dibenzylamino)-4-eicosanol, 59

According to the method of Example 26, from aldehyde 6 (600 mg, 2.24 mmol) and 1-bromohexadecane (1.37 mL, 4.49 mmol), alcohol 59 was obtained as a colorless oil (775 mg, 70% yield).

R_(f) 0.50 (hexane/EtOAc 9:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=7.1 Hz), 0.95 (t, 3H, J=7.1 Hz), 1.20–1.40 (m, 28H), 1.45–1.60 (m, 3H), 1.70–1.85 (m, 1H), 2.22 (br s, 1H), 2.62–2.68 (m, 1H), 3.62–3.73 (m, 5H), 7.24–7.34 (m, 10H);

¹³C NMR (75 MHz, CDCl3) δ 12.3, 14.1, 18.1, 22.6, 26.6, 29.3, 29.6, 29.7, 31.9, 34.4, 55.1, 62.7, 70.5, 126.9, 128.2, 128.9, 140.1;

ESMS calcd for C₃₄H₅₆NO (M+H) 494.4, found 494.5.

Example 58 (3S,4R)-3-Amino-4-eicosanol, 60

According to the method of Example 27, from N,N-dibenzylamine 59 (200 mg, 0.40 mmol), aminoalcohol 60 was obtained as a white solid (104 mg, 83% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.87 (t, 3H, J=6.9 Hz), 0.89 (t, 3H, J=6.9 Hz), 1.20–1.40 (m, 30H), 1.45–1.53 (m, 2H), 2.55–3.20 (m, 4H), 3.50–3.61 (m, 1H);

ESMS calcd for C₂₀H₄₄NO (M+H) 314.3, found 314.4.

Example 59 (3S,4R)-3-Amino-4-eicosanol hydrochloride, 61

According to the method of Example 32, from aminoalcohol 60 (30.0 mg, 0.17 mmol), hydrochloride 61 was obtained as a white solid (20.4 mg, 61% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=7.4 Hz), 1.04 (t, 3H, J=7.4 Hz), 1.25–1.50 (m, 30H), 1.55–1.80 (m, 2H), 3.04–3.12 (m, 1H), 3.70–3.80 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 10.5, 14.4, 21.3, 23.7, 27.1, 30.4, 30.6, 30.7, 30.8, 32.9, 33.0, 59.0, 71.4;

ESMS calcd for C₂₀H₄₄NO (M−Cl) 314.3, found 314.5.

Example 60 (3S,4R)-3-(N,N-Dibenzylamino)-4-heneicosanol, 62

According to the method of Example 26, from aldehyde 6 (610 mg, 2.28 mmol) and 1-bromoheptadecane (1.82 g, 5.70 mmol), alcohol 62 was obtained as a colorless oil (620 mg, 54% yield).

R_(f) 0.50 hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.86 (t, 3H, J=6.9 Hz), 0.94 (t, 3H, J=7.3 Hz), 1.20–1.40 (m, 30H), 1.45–1.55 (m, 3H), 1.70–1.85 (m, 1H), 2.24 (br s, 1H), 2.73 (td, 1H, J=7.0, 4.2 Hz), 3.60–3.75 (m, 5H), 7.22–7.36 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 12.3, 14.1, 18.1, 22.7, 26.7, 29.4, 29.6, 29.7, 31.9, 34.4, 55.2, 62.8, 70.6, 126.9, 128.3, 128.9, 140.1;

ESMS calcd for C₃₅H₅₈NO (M+H) 508.4, found 508.5.

Example 61 (3S,4R)-3-Amino-4-heneicosanol, 63

According to the method of Example 27, from N,N-dibenzylamine 62 (295 mg, 0.58 mmol), aminoalcohol 63 was obtained as a white solid (184 mg, 97% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=7.0 Hz), 0.94 (t, 3H, J=7.4 Hz), 1.20–1.40 (m, 32H), 1.45–1.60 (m, 2H), 1.79 (br s, 3H), 2.62–2.70 (m, 1H), 3.42–3.50 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 11.0, 14.1, 22.7, 25.0, 26.2, 29.3, 29.7, 29.8, 31.4, 31.9, 57.1, 74.1;

ESMS calcd for C₂₁H₄₆NO (M+H) 328.3, found 328.4.

Example 62 (3S,4R)-3-Amino-4-heneicosanol hydrochloride, 64

According to the method of Example 32, from aminoalcohol 63 (74 mg, 0.23 mmol), hydrochloride 64 was obtained as a white solid (51 mg, 62% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, * 6.9 Hz), 1.04 (t, 3H, J=7.4 Hz), 1.25–1.50 (m, 32H), 1.55–1.80 (m, 2H), 3.04–3.12 (m, 1H), 3.70–3.80 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 10.6, 14.5, 21.4, 23.7, 27.1, 30.5, 30.6, 30.7, 30.8, 33.0, 33.1, 59.0, 71.4;

ESMS calcd for C₂₁H₄₆NO (M−Cl) 328.3, found 328.4.

Example 63 (4S,5R)4-(N,N-Dibenzylamino)-5-eicosanol, 65

According to the method of Example 26, from aldehyde 11 (123 mg, 0.44 mmol) and 1-bromopentadecane (318 mg, 1.09 mmol), alcohol 65 was obtained as a colorless oil (161 mg, 75% yield).

R_(f) 0.53 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.89 (t, 3H, J=6.9 Hz), 0.91 (t, 3H, J=7.0 Hz), 1.20–1.40 (m, 28H), 1.40–1.55 (m, 3H), 1.70–1.80 (m, 1H), 2.22 (br S, 1H), 2.65–2.72 (m, 1H), 3.60–3.75 (m, 5H), 7.21–7.35 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 14.4, 20.6, 22.7, 26.7, 27.5, 29.4, 29.6, 29.6, 29.7, 31.9, 34.4, 55.2, 60.7, 70.7, 127.0, 128.3, 128.9, 140.1;

ESMS calcd for C₃₄H₅₆NO (M+H) 494.4, found 494.4.

Example 64 (4S,5R)-4-Amino-5-eicosanol, 66

According to the method of Example 27, from N,N-dibenzylamine 65 (37 mg, 0.075 mmol), aminoalcohol 66 was obtained as a white solid (17 mg, 72% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.7 Hz), 0.93 (t, 3H, J=6.7 Hz), 1.20–1.40 (m, 30H), 1.45–1.55 (m, 2H), 2.75–2.80 (m. 1H), 3.40–3.45 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 19.7, 22.7, 26.2, 29.4, 29.7, 31.4, 31.9, 34.4, 55.0, 74.4;

ESMS calcd for C₂₀H₄₄NO (M+H) 314.3, found 314.3.

Example 65 (4S,5R)-4-Amino-5-eicosanol hydrochloride, 67

According to the method of Example 32, from aminoalcohol 66 (9 mg, 0.03 mmol), hydrochloride 67 was obtained as a white solid (3 mg, 30% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.9 Hz), 0.99 (t, 3H, J=7.0 Hz), 1.20–1.40 (m, 28H), 1.40–1.65 (m, 4H), 3.08–3.18 (m, 1H), 3.65–3.75 (m, 1H);

ESMS calcd for C₂₀H₄₄NO (M−Cl) 314.3, found 314.5.

Example 66 (3S,4R)-3-(N,N-Dibenzylamino)-2-methyl-4-nonadecanol, 68

According to the method of Example 26, from aldehyde 14 (447 mg, 1.59 mmol) and 1-bromopentadecane (1.16 g, 4.0 mmol), alcohol 68 was obtained as a colorless oil (340 mg, 43% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.93 (t, 3H, J=7.0 Hz), 0.96 (d, 3H, J=6.5 Hz), 1.25–1.40 (m, 29H), 1.55–1.70 (m, 2H), 2.19–2.27 (m, 1H), 2.56 (dd, 1H, J=9.7, 4.7 Hz), 2.84 (br d, 1H,. J=7.9 Hz), 3.55–3.65 (m, 1H), 3.79 (d, 2H, J=13.4 Hz), 3.9.0 (d, 2H, J=13.4 Hz), 7.25–7.38 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 20.8, 22.7, 23.2, 27.1, 28.2, 29.3, 29.6, 29.6, 31.9, 33.2, 56.3, 67.2, 70.3, 127.2, 128.4, 129.1, 139.9;

ESMS calcd for C₃₄H₅₆NO (M+H) 494.4, found 494.4.

Example 67 (3S,4R)-3-Amino-2-methyl-4-nonadecanol, 69

According to the method of Example 27, from N,N-dibenzylamine 68 (171 mg, 0.35 mmol), aminoalcohol 69 was obtained as a white solid (90 mg, 83% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.85 (t, 3H, J=7.0 Hz), 0.88 (d, 3H, J=6.7 Hz), 0.95 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 26H), 1.50–1.65 (m, 3H), 2.02 (br s, 3H), 2.41 (dd, 1H, J=7.9, 4.7 Hz), 3.54–3.62 (m, 1H);

¹³C NMR-(75 MHz, CDCl₃) δ 14.1, 19.2, 19.8, 22.6, 26.1, 29.3, 29.6, 29.7, 29.7, 30.4, 30.8, 31.9, 61.7, 71.5;

ESMS calcd for C₂₀H₄₄NO (M+H) 314.3, found 314.3.

Example 68 (3S,4R)-3-Amino-2-methyl-4-nonadecanol hydrocloride, 70

According to the method of Example 32, from aminoalcohol 69 (68.5 mg, 0.22 mmol), hydrochloride 70 was obtained as a white solid (55.5 mg, 73% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.7 Hz), 1.01 (d, 3H, J=6.7 Hz), 1.05 (d, 3H, J=6.7 Hz), 1.25–1.40 (m, 26H), 1.55–1.70 (m, 2H), 1.88–1.96 (m, 1H), 2.84 (dd, 1H, J=8.6, 4.1 Hz), 3.80–3.85 (m, 1H);

¹³C NMR (75 MHz, CDOD₃) δ 14.5, 19.5, 19.9, 23.7, 27.0, 28.7, 30.5, 30.6, 30.7, 30.8, 31.1, 33.1, 63.8, 69.5;

ESMS calcd for C₂₀H₄₄NO (M−Cl) 314.3, found 314.4.

Example 69 (3S,4S,5R)-4-(N,N-Dibenzylamino)-3-methyl-5-eicosanol, 71

According to the method of Example 26, from aldehyde 17 (470 mg, 1.59 mmol) and 1-bromopentadecane (0.63 mL, 3.18 mmol), alcohol 71 was obtained as a colorless oil (499 mg, 60% yield).

R_(f) 0.60 (hexane/EtOAc 9:1);

¹H NMR (300 MHz, CDCl₃) δ 0.85–0.90 (m, 6H), 0.98 (d, 3H, J=7.4 Hz), 1.25–1.40 (m, 27H), 1.55–1.60 (m, 2H), 1.86–1.97 (mi, 2H), 2.54–2.60 (m,2H), 3.58–3.68 (m, 1H), 3.70 (d, 2H, J=13.7 Hz), 3.85 (d, 2H, J=13.7 Hz), 7.25–7.38 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 11.3, 14.1, 16.1, 22.6, 26.8, 28.1, 29.3, 29.5, 29.6, 31.8, 33.4, 34.2, 56.1, 65.5, 70.3, 127.1, 128.3, 129.1, 138.9;

ESMS calcd for C₃₅H₅₈NO (M+H) 508.4, found 508.8.

Example 70 (3S,4S,5R)-4-Amino-3-methyl-5-eicosanol, 72

According to the method of Example 27, from N,N-dibenzylamine 71 (70 mg, 0.13 mmol), aminoalcohol 72 was obtained as a white solid (40 mg, 89% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.91–1.10 (m, 6H), 1.15–1.46 (m, 31H), 2.45–2.51 (m, 2H), 1.65–1.69 (m, 1H), 2.68–2.72 (m, 1H), 3.62–3.69 (m, 1H), 4.25–4.60 (m, 2H);

ESMS calcd for C₂₁H₄₆NO (M+H) 328.3, found 328.4.

Example 71 (3S,4S,5R)-4-Amino-3-methyl-5-eicosanol hydrochloride, 73

According to the method of Example 32, from aminoalcohol 72 (40 mg, 0.11 mmol), hydrochloride 73 was obtained as a white solid (32 mg, 78% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.9 Hz), 0.95 (t, 3H, J=6.9 Hz), 1.20–1.40 (m, 31H), 1.45–1.60 (m, 2H), 1.75–1.85 (m, 1H), 3.18–3.23 (m, 1H), 3.90–3.95 (m, 1H), 7.90–8.05 (br s, 3H);

¹³C NMR (75 MHz, CDCl₃) δ 10.5, 14.1, 15.6, 22.6, 25.3, 26.1, 29.3, 29.6, 29.7, 31.9, 33.7, 61.6, 70.1;

ESMS calcd for C₂₁H₄₆NO (M−Cl) 328.3, found 328.4.

Example 72 (2S,3R)-1-(4′-Benzyloxyphenyl)-2-(N,N-dibenzylamino)-3-octadecanol, 74

According to the method of Example 26, from aldehyde 20 (597 mg, 1.37 mmol) and 1-bromopentadecane (999 mg, 3.43 mmol), alcohol 74 was obtained as a colorless oil (496 mg, 56% yield).

R_(f) 0.50 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 0.90 (t, 3H, J=6.7 Hz), 1.25–1.40 (m, 26H), 1.55–1.70 (m, 2H), 1.96 (br s, 1H), 2.43 (dd, 1H, J=12.4, 5.2 Hz), 2.95–3.07 (m, 2H), 3.65 (d, 2H, J=13.8 Hz), 3.65–3.75 (m, 1H), 3.78 (d, 2H, J=13.8 Hz), 5.09 (s, 2H), 6.92 (d, 2H, J=8.6 Hz), 7.07 (d, 2H, J=8.6 Hz), 7.20–7.49 (m, 15H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 22.7, 26.4, 29.4, 29.5, 29.6, 29.7, 31.0, 31.9, 34.6, 55.1, 63.2, 70.1, 71.6, 114.8, 126.9, 127.4, 127.9, 128.2, 128.6, 128.8, 130.2,132.8, 137.2, 139.8, 157.1;

ESMS calcd for C₄₅H₆₂NO₂ (M+H) 648.5, found 648.5.

Example 73 (2S,3R)-2-Amino-1-(4′-hydroxyphenyl)-3-octadecanol, 75

According to the method of Example 27, from N,N-dibenzylamine 74 (140 mg, 0.22 mmol), aminoalcohol 75 was obtained as a white solid (80 mg, 98% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (d, 3H, J=6.6 Hz), 1.25–1.40 (m, 26H), 1.50–1.65 (m, 21), 2.35–2.44 (m, 1H), 2.81–2.92 (m, 2H), 3.45–3.50 (m, 1H), 6.73 (d, 2H, J=8.2 Hz), 7.03 (d, 2H, J=8.2 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.5, 23.7, 27.2, 30.5, 30.8, 30.8, 33.1, 33.4, 38.3, 58.7, 74.8, 116.4, 130.9, 131.2, 157.1;

ESMS calcd for C₂₄H₄₄NO₂ (M+H) 378.3, found 378.3.

Example 74 (2S,3R)-2-Amino-1-(4′-hydroxyphenyl)-3-octadecanol hydrochloride, 76

According to the method of Example 32, from aminoalcohol 75 (43 mg, 0.11 mmol), hydrochloride 76 was obtained as a white solid (10 mg, 21% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 26H), 1.45–1.60 (m, 2H), 2.72 (dd, 1H, J=14.3, 9.3 Hz), 2.92 (dd, 1H, J=14.3, 5.4 Hz),:3.39 (ddd, 1H, J=9.1, 5.5, 3.2 Hz), 3.66–3.75 (m, 1H), 6.78 (d, 2H, J=8.6 Hz), 7.10 (d, 2H, J=8.6 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.5, 23.8, 27.1, 30.5, 30.6, 30.7, 30.7, 30.8, 33.1, 33.6, 59.0, 71.3, 116.8, 127.9, 131.3, 157.9;

ESMS calcd for C₂₄H₄₄NO₂ (M−Cl) 378.3, found 378.3.

Example 75 (4S,5R)-1,4-Bis-(N,N-dibenzylamino)-5-eicosanol, 77

According to the method of Example 26, from aldehyde 23 (503 mg, 1.05 mmol) and 1-bromopentadecane (768; mg, 2.64 mmol), alcohol 77 was obtained as a colorless oil (350 mg, 48% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.90 (t, 3H, J=6.7 Hz), 1.25–1.40 (m, 28H), 1.40–1.60 (m, 2H), 1.60–1.75 (m, 2H), 1.97 (br s, 1H), 2.43 (t, 2H, J=6.7 Hz), 2.56–2.62 (m, 1H), 3.57 (s, 4H), 3.61 (d, 2H, J=13.8 Hz), 3.65–3.75 (m, 1H), 3.67 (d, 2H, J=13.8 Hz), 7.20–7.40 (m, 20H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 22.7, 23.1, 25.1, 26.6, 29.4, 29.6, 29.7, 31.9, 34.6, 53.9, 55.1, 58.4, 61.2, 70.9, 126.8, 127.0, 128.1, 128.3, 128.8, 128.9, 139.8, 140.1;

ESMS calcd for C₄₈H₆₉N₂O (M+H) 689.5, found 689.5.

Example 76 (4S,5R)-1,4-Diamino-5-eicosanol, 78

According to the method of Example 27, from bis-(N,N-dibenzylamine) 77 (105 mg, 0.15 mmol), diaminoalcohol 78 was obtained as a white solid (45 mg, 91% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.88 (d, 3H, J=6.7 Hz), 1.25–1.45 (m, 28H), 1.60–1.75 (m, 4H), 2.65–2.85 (m, 3H), 3.42–3.52 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 14.4, 23.7, 26.9, 27.2, 28.8, 30.5, 30.8, 33.1, 33.4, 41.1, 56.9, 74.6;

ESMS calcd for C₂₀H₄₅N₂O (M+H) 329.3, found 329.3.

Example 77 (4S,5R)-1,4-Diamino-5-eicosanol dihydrochloride, 79

According to the method of Example 32, from diaminoalcohol 78 (40 mg, 0.12 mmol) dihydrochloride 79 was obtained as a white solid (30 mg, 61% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (d, 3H, J=6.5 Hz), 1.25–1.40 (m, 26H), 1.45–1.60 (m, 3H), 1.70–1.95 (m, 3H), 2.98 (t, 2H, J=7.0 Hz), 3.20–3.25 (m, 1H), 3.72–3.80 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 14.5, 23.7, 25.1, 25.5, 27.1, 30.5, 30.7, 30.8, 30.8, 33.1, 33.3, 40.4, 56.9, 71.5;

ESMS calcd for C₂₀H₄₅N₂O (M−HCl₂) 329.3, found 329.4.

Example 78 (2R,3S)-2-(N,N-Dibenzylamino)-3-octadecanol, 80

According to the method of Example 26, from aldehyde 26 (445 mg, 1.76 mmol) and 1-bromopentadecane (1.28 g, 4.39 mmol), alcohol 80 was obtained as a colorless oil (422 mg, 52% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.91 (t, 3H, J=6.9 Hz), 1.12 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 26H), 1.65–1.75 (m, 2H), 1.85 (br s, 1H), 2.73 (quint, 1H, J=6.4 Hz), 3.49 (d, 2H, J=13.9 Hz), 3.57–3.65 (m, 1H), 3.78 (d, 2H, J=13.8 Hz), 7.21–7.38 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.6, 14.1, 22.7, 25.9, 29.3, 29.6, 29.7, 31.9, 34.4, 54.8, 57.3, 73.6, 126.9, 128.2, 128.8, 140.2;

ESMS calcd for C₃₂H₅₂NO (M+H) 466.4, found 466.4.

Example 79 (2R,3S)-2-Amino-3-octadecanol, 81

According to the method of Example 27, from N,N-dibenzylamine 80 (256 mg, 0.55 mmol), aminoalcohol 81was obtained as a white solid (175 mg, 92% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=7.0 Hz), 1.02 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 26H), 1.45–1.55 (m, 2H), 1.85 (br s, 3H), 2.94–3.04 (m, 1H), 3.42–3.52 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 16.3, 22.7, 26.2, 29.3, 29.7, 31.9, 32.5, 50.4, 74.2;

ESMS calcd for C18H₄₀NO (M+H) 286.3, found 286.2.

Example 80 (2S,3R)-O-Acetyl-2-(N,N-dibenzylamino)-3-octadecanol, 82

To a solution of alcohol 39 (48.5 mg. 0.104 mmol) in CH₂Cl₂ (1.0 mL) at room temperature, pyridine (25 μL, 0.313 mmol), Ac₂O (29 μL, 0.313 mmol) and DMAP (ca. 5 mg, cat.) were added. The reaction was stirred for 4 h, and then the solvents were evaporated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 10: 1) to obtain acetate 82 as a colorless oil (46 mg, 87% yield).

R_(f) 0.62 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.91 (t, 3H, J=6.8 Hz), 1.07 (d, 3H, J=6.6 Hz), 1.20–1.35 (m, 26H), 1.40–1.50 (m, 1H), 1.75–1.85 (m, 1H), 2.02 (s, 3H), 2.81 (quint, 1H, J=7.1 Hz), 3.46 (d, 2H, J=13.9 Hz), 3.76 (d, 2H, J=13.9 Hz), 5.11 (dt, 1H, J=7.5, 4.2 Hz), 7.22–7.39 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.7, 14.1, 21.2, 22.7, 24.8, 29.3, 29.5, 29.6, 29.7, 31.9, 32.0, 54.2, 54.7, 75.2, 126.8, 128.1, 12.8, 140.0, 170.8;

ESMS calcd for C₃₄H₅₄NO₂ (M+H) 508.4, found 508.5.

Example 81 (2S,3R)-2-(N-Acetylamino)-3-octadecanol, 83

According to the method of Example 27, from N,N-dibenzylamine 82 (41 mg, 0.081 mmol), acetamide 83 was obtained as a white solid (13 mg, 49% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.89 (t, 3H, J=7.1 Hz), 1.09 (d, 3H, J=6.8 Hz), 1.20–1.35 (m, 26H), 1.45–1.55 (m, 2H), 1.99 (s, 3H), 2.15 (br s, 1H), 3.60–3.65 (m, 1H), 4.00 (dquint, 1H, J=7.4, 2.4 Hz), 5.84 (br d, 1H, J=7.1 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 13.9, 14.1, 22.7, 23.5, 26.0, 29.4, 29.6, 29.7, 31.9, 33.6, 49.5, 74.2, 82.4, 170.0;

ESMS calcd for C₂₀H₄₁NO₂Na (M+Na) 350.3, found 350.3.

Example 82 (2S,3R)-2-(N,N-Dibenzylamino)-3-(methoxy)-octadecane, 84

To a solution of alcohol 39 (322 mg, 0.69 mmol) in DMF (3.5 mL) at room temperature, NaH (60% mineral dispersion, 69 mg, 1.73 mmol) and MeI (0.22 mL, 3.46 mmol) were added. After stirring for 16 h, the mixture was quenched with H₂O (15 mL), extracted with Et₂O (3×15 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 15:1) to obtain 84 as a colorless oil (110 mg, 33% yield).

R_(f) 0.56 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 0.94 (t, 3H, J=6.7 Hz), 1.08 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 26H), 1.55–1.70 (m, 2H), 2.74 (quint, 1H, J=6.7 Hz), 3.27 (q, 1H, J=6.4 Hz), 3.36 (s, 3H), 3.50 (d, 2H, J=13.8 Hz), 3.77 (d, 2H, J=13.8 Hz), 7.23–7.42 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.2, 14.1, 22.7, 24.4, 29.4, 29.7, 29.7, 29.7, 30.0, 30.6, 31.9, 54.3, 54.7, 57.4, 83.7, 126.7, 128.1, 128.8, 140.4;

ESMS calcd for C₃₃H₅₄NO (M+H) 480.4, found 480.7.

Example 83 (2S,3R)-2-Amino-3-(methoxy)-octadecane, 85

According to the method of Example 27, from N,N-dibenzylamine 84 (54 mg, 0.11 mmol), amine 85 was obtained as a white solid (14 mg, 42% yield).

R_(f) 0.10 (hexane/EtOAc 1:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.6 Hz), 1.03 (d, 3H, J=6.7 Hz), 1.20–1.35 (m, 26H), 1.40–1.55 (m, 2H); 1.96 (br s, 2H), 2.94–3.00 (m, 1H), 3.03–3.10 (m, 1H), 3.38 (s, 3H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 18.3, 22.7, 26.0, 29.1, 29.3, 29.6, 29.6, 29.7, 29.9, 31.9, 47.9, 57.9, 75.0, 85.7;

ESMS calcd for C₁₉H₄₂NO (M+H) 300.3, found 300.5.

Example 84 (2S,3S)-2-(N,N-Dibenzylamino)-3-chloro-octadecane, 86

To a cold (0° C.) solution of alcohol 39 (24 mg, 0.051 mmol) in 1 mL of pyridine, POCl₃ (0.019 mL, 0.206 mmol) was added dropwise. After stirring at room temperature for 3 h, 0.2 mL of H₂O were added and the solvent was evaporated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 10:1) to give chloride 86 as a colorless oil (14 mg, 56% yield).

R_(f) 0.56 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 0.89 (t, 3H, J=6.6 Hz), 1.20–1.55 (m, 30H), 2.00–2.10 (m, 1H), 2.87 (quint, 1H, J=7.0 Hz), 3.47 (d, 2H, J=13.8 Hz), 3.75 (d, 2H, J=13.6 Hz), 3.98 (td, 1H, J=8.1, 3.5 Hz), 7.21–7.36 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 10.2, 14.1, 22.7, 26.0, 29.2, 29.4, 29.5, 29.6, 29.7, 31.9, 35.6, 54.3, 57.3, 66.9, 126.9, 128.2, 128.8, 139.8;

ESMS calcd for C₃₂H₅₁ClN (M+H) 484.4, found 484.3.

Example 85 (2S,3S)-2-Amino-3-chloro-octadecane, 87

According to the method of Example 27, from N,N-dibenzylamine 86 (13 mg, 0.027 mmol), amine 87 was obtained as a white sohd (3 mg, 37% yield).

R_(f) 0.10 (EtOAc); ¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=6.6 Hz), 1.12 (d, 3H, J=6.6 Hz), 1.20–1.70 (m, 30H), 3.09 (qd, 1H, J=6.2, 3.4 Hz), 3.90 (td, 1H, J=6.5, 3.5 Hz);

ESMS calcd for C₁₈H₃₈N (M−Cl) 268.3, found 268.2.

Example 86 (2S,3R)-2-(N,N-Dibenzylamino)-O-(dimethylphosphate)-3-octadecanol, 88

To a solution of alcohol 39 (44 mg, 0.095 mmol) and CBr₄ (47 mg, 0.142 mmol) in 0.3 mL of pyridine, (MeO)₃P (0.022 mL, 0.189 mmol) was added dropwise. After stirring at room temperature for 24 h, the mixture was diluted with EtOAc (10 mL), washed successively with 5% HCl (10 mL), NaHCO₃ (10 mL, sat. aq.) and brine (10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 10:1 to 2:1) to give dimethyl phosphate 88 as a colorless oil (20 mg, 37% yield) together with unreacted alcohol (25 mg, 57% yield).

R_(f) 0.31 (hexane/EtOAc 2:1);

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=6.5 Hz), 1.16 (d, 3H, J=6.5 Hz), 1.20–1.40 (m, 26H), 1.65–1.80 (m, 2H), 2.84 (quint, 1H, J=6.9 Hz), 3.40 (d, 2H, J=13.8 Hz), 3.69 (dd, 3H, J=2.3, 0.5 Hz), 3.73 (dd, 3H, J=2.3, 0.5 Hz), 3.73 (d, 2H, J=13.6 Hz), 4.47 (ddd, 1H, J=12.8, 7.4, 4.9 Hz), 7.20–7.34 (m, 10H);

¹³C NMR (75 MHz, CDCl₃) δ 8.5, 14.1, 22.7, 23.4, 29.3, 29.5, 29.6, 29.6, 29.7, 31.9, 32.6, 54.0 (d), 54.1 (d), 54.2, 81.7 (d), 126.9, 128.2, 128.9, 139.8;

ESMS calcd for C₃₄H₅₇NO₄P (M+H) 574.4, found 574.4.

Example 87 (2S,3R)-2-Amino-O-(dimethylphosphate)-3-octadecanol, 89

According to the method of Example 27, from N,N-dibenzylamine 88 (16 mg, 0.028 mmol), amine 89 was obtained as a white solid (6 mg, 55% yield).

R_(f) 0.32 (EtOAc/MeOH 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=6.6 Hz), 1.08 (d, 3H, J=6.6 Hz), 1.20–1.40 (m, 26H), 1.45–1.55 (m, 1H), 1.60–1.70 (m, 1H), 1.97 (br s, 2H), 3.12–3.20 (m, 1H), 3.76 (s, 3H), 3.80 (s, 3H), 4.24–4.34 (m, 1H);

ESMS calcd for C₂₀H₄₅NO₄P (M+H) 394.3, found 394.3.

Example 88 (2S,3S)-2-(N-Benzyloxycarbonylamino)-3-octadecanol, 90

According to the method of Example 26, from aldehyde 28 (640 mg, 3.1 mmol) and 1-bromopentadecane (5.0 g, 17.2 mmol), alcohol 90 was obtained as a colorless oil (690 mg, 53% yield).

¹H NMR (500 MHz, CDCl₃) δ 0.88 (t, 3H, J=7.1 Hz), 1.20 (d, 3H, J=6.8 Hz), 1.20–1.35 (m, 26H), 1.40–1.50 (m, 2H), 1.74 (br s, 1H), 3.48–3.52 (m, 1H), 3.70–3.75 (m, 1H), 4.90–4.95 (m, 1H), 5.10 (s, 2H), 7.30–7.36 (m, 5H).

Example 89 (2S,3S)-2-Amino-3-octadecanol, 91

To a solution of N-benzyloxycarbonylamine 90 (330 mg, 0.79 mmol) in MeOH (40 mL) at room temperature, Pd—C (10% wt, 100 mg, 0.09 mmol) was added. The mixture was purged with a stream of dry Ar, and then H₂. The reaction was stirred overnight under a H₂ atmosphere (1 atm). The catalyst was filtered off through a 0.45 μm teflon filter in polypropylene housing, washing the filter with MeOH (50 mL) and the solvent was evaporated in vacuo. The crude was purified by column chromatography on silica (90:10 CH₂Cl₂/MeOH to 100% MeOH) to obtain aminoalcohol 91 as a white solid (200 mg, 89% yield).

¹H NMR (500 MHz, CD₃OD) δ 0.80 (t, 3H, J=7.2 Hz), 0.98 (d, 3H, J=6.5 Hz), 1.15–1.30 (m, 26H); 1.40–1.45 (m, 2H), 2.62–2.65 (m, 1H), 3.10–3.15 (m, 1H);

¹³C NMR (125 MHz, CD₃OD) δ 14.8, 19.2, 24.1, 27.2, 20.9, 31.1, 33.5, 35.0, 53.0, 77.1;

ESMS calcd for C₁₈H₄₀NO (M+H) 286.3, found 286.4.

Example 90 (3S,4S)-3-(N-Benzyloxycarbonylamino)-4-nonadecanol, 92

According to the method of Example 26, from aldehyde 8 (680 mg, 3.1 mmol) and 1-bromopentadecane (6.55 g, 22.5 mmol), alcohol 92 was obtained as a colorless oil (800 mg, 60% yield).

¹H NMR (500 MHz, CDCl₃) δ 0.88 (t, 3H, J=7.1 Hz), 0.96 (t, 3H, J=7.4 Hz), 1.20–1.35 (m, 26H), 1.40–1.45 (m, 2H), 1.55–1.60 (m, 1H), 1.65–1.70 (m, 1H), 3.46–3.52 (m, 1H), 3.60–3.65 (m, 1H), 4.91 (d, 1H, J=9.3 Hz), 5.11 (s, 2H), 7.30–7.36 (m, 5H).

Example 91 (3S,4S)-3-Amino-4-nonadecanol, 93

According to the method of Example 89, from N-benzyloxycarbonylamine 92 (230 mg, 0.53 mmol), aminoalcohol 93 was obtained as a white solid (140 mg, 89% yield).

¹H NMR (500 MHz, CD₃OD) δ 0.80 (t, 3H, J=7.1 Hz), 0.93 (t, 3H, J=7.5 Hz), 1.15–1.25 (m, 26H), 1.30–1.40 (m, 2H), 1.40–1.50 (m, 1H), 1.65–1.75 (m, 1H), 2.80–2.85 (m, 1H), 3.45–3.50 (m, 1H);

¹³C NMR (125 MHz, CD₃OD) δ 10.0, 14.4, 23.7, 24.1, 26.6, 30.5, 30.6, 30.8, 33.1, 34.9, 58.8, 70.5;

ESMS calcd for C₁₉H₄₂NO (M+H) 300.3, found 300.4.

Example 92 (2S,3-S)-2-(N-tert-Butoxycarbonylamino)-3-octadecanol, 94

To a solution of aminoalcohol 91 (46 mg, 0.16 mmol) in CH₂Cl₂ (1.6 mL) at room temperature, Boc₂O (42 mg, 0.19 mmol) was added. After stirring for 3.5 h, the solvent was removed in vacuo to obtain 94 as a white solid (62 mg, 100% yield).

R_(f) 0.35 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.86 (t, J=6.5 Hz, 3H), 1.15 (d, J=6.8 Hz, 3H), 1.20–1.40 (m, 26H), 1.43 (s, 9H), 1.45–1.60 (m, 2H), 3.40–3.50 (m, 1H), 3.55–3.65 (m, 1H), 4.75 (d, 1H, J=8.8 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 18.3, 22.7, 25.6, 27.4, 28.4, 29.3, 29.6, 29.6, 29.7, 31.9, 34.2, 50.5, 74.9, 156.2.

Example 93 (2S,3R)-3-Azido-2-(N-tert-butoxycarbonylamino)-octadecane, 95

To a cold (0° C.) solution of alcohol 94 (48 mg, 0.12 mmol) in CH₂Cl₂ (1.25 mL), Et₃N (52 μL, 0.37 mmol) and MsCl (24 μL, 0.31 mmol) were added. After stirring for 2 h, the mixture was quenched with H₂O (10 mL), extracted with CH₂Cl₂ (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude mesylate was dissolved in DMF (0.65 mL) and NaN₃ (40.5 mg, 0.62 mmol) was added. The mixture was stirred at 120 C. for 3 h and then quenched with H₂O (10 mL), extracted with Et₂O (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 10:1 to 5:1) to obtain azide 95 as a colorless oil (25 mg, 49% yield).

R_(f) 0.31 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.6 Hz), 1.06 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 26H), 1.44 (s, 9H), 1.45–1.55 (m, 2H), 3.50–3.58 (m, 1H), 3.70–3.80 (m, 1H), 4.68 (br d, 1H, J=7.7 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 14.4, 22.7, 26.5,.28.2, 28.4, 29.3, 29.4, 29.4, 29.5, 29.6, 29.6, 29.7, 31.4, 31.9, 49.3, 66.5, 155.0.

Example 94 (2S,3R)-3-Amino-2-(N-tert-butoxycarbonylamino)-octadecane, 96

To a solution of azide 95 (25 mg, 0.06 mmol) in MeOH (1.5 mL) at room temperature, Pd—C (10% wt, 16 mg, 0.015 mmol) was added. The mixture was purged with a stream of dry Ar, and then H₂. The reaction was stirred overnight under a H₂ atmosphere (1 atm). The catalyst was filtered off through a 0.45 μm teflon filter in polypropylene housing, washing the filter with MeOH (15 mL) and the solvent was evaporated in vacuo to obtain amine 96 as a white solid (22 mg, 94% yield).

R_(f) 0.12 (hexane/EtOac 1.10); ¹H NMR (300 MHz, CDCl₃) δ 0.86 (t, 3H, J=6.5 Hz), 1.02 (d, 3H, J=6.7 Hz), 1.20–1.40 (m, 26H), 1.43 (s, 9H), 1.45–1.55 (m, 2H), 2.0.5 (br s, 2H), 2.72–2.82 (m, 1H), 3.60–3.70 (m, 1H), 5.00–5.10 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 22.7, 26.5, 28.4, 29.3, 29.7, 31.9, 34.8, 49.7, 54.8, 155.4;

ESMS calcd for C₂₃H₄₉N₂O₂ (M+H) 385.4, found 385.4.

Example 95 (2S,3R)-2,3-Diamino-octadecane dihydrochloride, 97

To a solution of N-Boc derivative 96 (22 mg, 0.057 mmol) in dioxane (0.4 mL), anhydrous HCl solution in dioxane (5.3M, 0.43 mL, 2.29 mmol) was added. After stirring at room temperature for 5 h, the solvent was removed in vacuo. The resulting solid was washed with dioxane to obtain dihydrochloride 97 as a white solid (11.5 mg, 56% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.4 Hz), 1.20–1.45 (m, 26H), 1.42 (d, 3H, J=7.0 Hz), 1.65–1.80 (m, 2H), 3.42–3.48 (m, 1H), 3.58–3.66 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 14.3, 14.4, 23.7, 26.3, 30.4, 30.5, 30.7, 30.7, 30.8, 33.1, 55.1;

ESMS calcd for C₁₈H₄₁N₂ (M−HCl₂) 285.3, found 285.3.

Example 96 (2S,3R)-2-(N-tert-Butoxycarbonylamino)-3-octadecanol, 98

According of the method of Example 92, from aminoalcohol 1 (82.5 mg, 0.30 mmol) N-Boc derivative 98 was obtained as a white solid (110 mg, 95% yield).

R_(f) 0.35 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.9 Hz), 1.09 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 26H), 1.45 (s, 9H), 1.49–1.60 (m, 2H), 2.01–2.09 (m, 1H), 3.55–3.69 (m, 3H), 4.61–4.72 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 14.2, 22.6, 26.0, .28.3, 29.3, 29.6, 31.9, 33.4, 50.5, 74.4, 172.1;

ESMS calcd for C₂₃H₄₇NO₃Na (M+Na) 408.4, found 408.3.

Example 97 (2S,3R)-2-(N-tert-Butoxycarbonylamino)-O(2,2,2-trifluoroacetyl)-3-octadecanol, 99

To a solution of alcohol 98 (54 mg, 0.14 mmol) in CH₂Cl₂ (6.0 mL) at room temperature, trifluoroacetic anhydride (28 μL, 0.14 mmol), pyridine (22 μL) 0.42 mmol) and DMAP (1.7 mg, 0.01 mmol) were added. After stirring for 1 h, the reaction was quenched with H₂O (10 mL), extracted with CH₂Cl₂ (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/AcOEt 9:1) to obtain trifluoroacetate 99 as a white solid (17 mg, 25% yield).

R_(f) 0.24 (hexane/AcOEt 9:1);

¹H NMR (300 MHz, CD₃OD) δ 0.80 (t, 3H, J=6.5 Hz), 1.08 (d, 3H, J=6.5 Hz) 1.18–1.36 (m, 26H), 1.41 (s, 9Hi), 1.52–1.61 (m, 2H), 3.87–3.92 (m, 1H), 4.39–4.44 (m, 1H), 4.98–5.21 (m, 1H);

ESMS calcd for C₂₅H₄₆F₃NO₄Na (M+Na) 504.3, found 504.4.

Example 98 (2S,3R)-2-Ammonium-O-(2,2,2-trifluoroacetyl)-3-octadecanol trifluoroacetate, 100

To a solution of N-Boc derivative 99 (17 mg, 0.03 mmol) in CH₂Cl₂ (4 mL) at room temperature, trifluoroacetic acid (1.0 mL) was added. After stirring for 1 h, the solvents were removed in vacuo to obtain 100 as a white solid (16 mg, 94% yield).

R_(f) 0.24 (hexane/AcOEt 9:1);

¹H NMR (300 MHz, CD₃OD) δ 0.80 (t, 3H, J=6.1 Hz), 1.18–1.25 (m, 26H), 1.28 (d, 3H, J=6.5Hz), 1.49–1.56 (m, 1H), 1.64–1.69 (m, 1H), 3.51 (m, 1H), 5.27 (m, 1H), 7.94 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 12.1, 21.4, 22.7, 25.9, 26.2, 26.3, 26.4, 26.6, 27.4,28.9,49.7, 79.0, 101.3, 111.4 161.1;

ESMS calcd for C₁₈H₃₉NO (M−C₄F₆O₃) 286.5, found 286.2.

Example 99 (2S,3R)-O-Acetyl 2-(N-tert-butoxycarbonylamino)-3-octadecanol, 101

According of the method of Example 80, from alcohol 98 (20 mg, 0.052 mmol), acetate 101 was obtained as a white solid (18.5 mg, 83% yield).

R_(f) 0.47 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.9 Hz), 1.08 (d, 3H, J=6.9 Hz), 1.20–1.35 (m, 26H), 1.43 (s, 9H), 1.45–1.55 (m, 2H), 2.06 (s, 3H), 3.79–3.89 (m, 1H), 4.60 (br d, 1H, J=7.7 Hz), 4.85 (dt, 1H, J=7.2, 4.9 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 15.3, 21.1, 22.7, 25.5, 28.4, 29.3, 29.4, 29.5, 29.6, 29.6, 29.7, 30.7, 31.9, 48.3, 79.3, 155.1, 171.0;

ESMS calcd for C₂₅H₄₉NO₄Na (M+Na) 450.4, found 450.4.

Example 100 (2S,3R)-O-Acetyl-2-amino-3-octadecanol hydrochloride, 102

According to the method of Example 95, from N-Boc derivative 101 (13.7 mg, 0.032 mmol) hydrochloride 102 was obtained as a white solid (9 mg, 77% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.6 Hz), 1.20–1.40 (m, 29H), 1.55–1.65 (m, 2H), 2.12 (s, 3H), 3.49 (qd, 1H, J=6.7, 2.4 Hz), 5.07 (ddd, 1H, J: 8.7, 5.0, 2.6 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 12.9, 14.5, 20.9, 23.8, 26.5, 30.3, 30.5, 30.5, 30.7, 30.8, 31.3, 33.1, 51.1, 74.3, 172.5;

ESMS calcd for C₂₀H₄₂NO₂ (M−Cl) 328.3, found 328.3.

Example 101 (2S,3S)-3-Azido-2-(N-tert-butoxycarbonylamino)-octadecane, 103

According to the method of Example 93, from alcohol 98 (50 mg, 0.13 mmol), azide 103 was obtained as a colorless oil (39 mg, 73% yield).

R_(f) 0.64 (hexane/EtOAc 10:1);

¹H NMR (300 MHz, CD₃OD) δ 0.87 (t, 3H, J=6.8 Hz), 1.18 (d, 3H, J=6.8 Hz), 1.20–1.39 (m, 26H), 1.43 (s, 9H), 1.53–1.61 (m, 2H), 3.30–3.36 (m, 1H), 3.55–3.97 (m, 1H), 4.50 (d, 1H, J=9.2 Hz);

ESMS calcd for C₂₃H₄₆N₄O₂Na (M+Na) 433.3, found 433.4.

Example 102 (2S,3S)-3-Amino-2-(N-tert-butoxycarbonylamino)-octadecane, 104

According to the method of Example 94, from azide 103 (15 mg, 0.03 mmol), amine 104 was obtained as a colorless oil (13 mg, 92% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.87 (t, 3H, J=6.8 Hz), 1.10 (d, 3H, J=6.8 Hz), 1.21–1.40 (m, 26H), 1.43 (s, 9H), 1.45–1.47 (m, 2H), 2.70–2.75 (m, 1H), 3.60–3.55 (m, 1H), 4.90 (d, 1H, J=6.8 Hz);

ESMS calcd for C₂₃H₄₉N₂O₂ (M+H) 385.4, found 385.4.

Example 103 (2S,3 S)-2,3-Diamino-octadecane dihydrochloride, 105

According to the method of Example 95, from N-Boc derivative 104 (13 mg, 0.03 mmol), dihydrochloride 105 was obtained as a white solid (11 mg, 75% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.8 Hz), 1.35 (d, 3H, J=6.8 Hz), 1.25–1.40 (m, 26H), 1.56–1.72 (m, 2H), 3.49–3.56 (m, 1H), 3.70–3.74 (m, 1H);

¹³C NMR (75 MHz, CD₃OD) δ 13.1, 14.4, 22.7, 26.5, 27.8, 30.5, 30.8, 33.1, 54.1;

ESMS calcd for C₁₈H₄₁N₂ (M−HCl₂) 285.3, found 285.4.

Example 104 (2S,3R)-2-(N,N-Dimethylamino)-3-octadecanol, 106

A mixture of aminoalcohol 1 (100 mg, 0.35 mmol), formaldehyde (37% w/w, aq. 142 mg, 1.75 mmol), NaB(OAc)₃H (370 mg, 1.75 mmol) and (CH₂Cl)₂ (2 mL) was stirred at room temperature for. 3 h. The reaction was quenched by the addition of NaHCO₃ (15 mL, sat. aq.) and extracted with EtOAc (3×25 mL). The combined extracts were dried over Na₂SO₄ and concentrated in vacuo to give 106 as a white solid (83 mg, 75% yield).

¹H NMR (500 MHz, CD₃OD) δ 0.80 (t, 3H, J=7.1 Hz), 0.92 (d, 3H, J=6.7 Hz), 1.15–1.25 (m, 26H), 1.30–1.40 (m, 2H), 2.19 (s, 6H), 2.30–2.35 (m, 1H), 3.60–3.65 (m, 1H);

¹³C NMR (125 MHz, CD₃OD) δ 8.7, 14.9, 24.2, 27.7, 30.9, 31.2, 33.5, 36.8, 42.2, 65.0, 73.3;

ESMS calcd for C₂₀H₄₄NO (M+H) 314.3, found 314.4.

Example 105 (4S,5R)-4-Methyl-5-(n-pentadecyl)-1,3-oxazolidinone, 107

A mixture of aminoalcohol 1 (150 mg, 0.53 mmol) and carbonyl diimidazole (94 mg, 0.58 mmol) in THF (10 mL) was stirred at 60° C. for 3 h. Then, the solvent was removed in vacuo and the residue was dissolved in CH₂Cl₂ (40 mL), washed successively with HCl (2N, 40 mL), H₂O (40 mL) and brine (40 mL), dried over Na₂SO₄ and concentrated in vacuo to give oxazolidinone 107 as a white solid (160 mg, 98% yield).

R_(f) 0.21 (hexane/EtOAc 2:1);

¹H NMR (300 MHz, CD₃OD) δ 0.80 (t, 3H, J=7.0 Hz), 1.02 (d, 3H, J=6.5 Hz), 1.15–1.30,(m, 26H), 1.40–1.55 (m, 2H), 3.81 (quint, 1H, J=6.5 Hz), 4.44–4.52 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 20.7, 22.7, 24.8, 29.3, 29.4, 29.4, 29.5, 29.7, 31.9, 34.1, 53.5, 84.2, 158.7;

ESMS calcd for C₁₉H₃₇NO₂Na (M+Na) 334.3, found 334.3.

Example 106 (2S,3R)-2-(N-Methylamino)-3-octadecanol, 108

To a cold (0° C.) solution of 107 (160 mg, 0.52 mmol) in THF(20 mL), LiAlH₄ (1M in THF, 1.04 mL, 1.04 mmol), was added dropwise. The mixture was stirred overnight at room temperature. A further portion of LiAlH₄ (1.04 mL, 1.04 mmol) was added and the reaction left for 2 more days. The reaction was quenched with H₂O containing a few drops of NH₄OH (20 mL) and extracted with EtOAc (3×20 mL). The combined extracts were successively washed with. H₂O (30 mL) and brine (30 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (50% to 75% CH₂Cl₂/hexane to 100% CH₂Cl₂ to 10% MeOH/CHCl₃ and a few drops of NH₄OH) to give 108 as a white solid (35 mg, 23% yield).

¹H NMR (500 MHz, CD₃OD) δ 0.80 (t, 3H, J=7.1 Hz), 0.92 (d, 3H, J=6.7 Hz), 1.15–1.25 (m, 26H), 1.30–1.45 (m, 2H), 2.19 (s, 3H), 2.50–2.55 (m, 1H), 3.55–3.60 (m, 1H);

¹³C NMR (125 MHz, CD₃OD) δ 13.3, 14.9, 24.2, 27.8, 30.9, 31.2, 33.5, 34.7, 36.8, 42.3, 60.5, 73.1;

ESMS calcd for C₁₉H₄₂NO (M+H) 300.3, found 300.3.

Example 107 (2S,3R)-2-Amino-N-(phenylthiocarbamoyl)-3-octadecanol, 109

To a solution of aminoalcohol 1 (197 mg, 0.69 mmol) in THP (3.5 mL) at room temperature, PhNCS (0.165 mL, 1.38 mmol) was added. The reaction was stirred for 1 h, and then the solvents were evaporated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 5:1 to 2:1) to give phenylthiourea 109 as a white solid (246 mg, 85% yield).

R_(f) 0.29 (hexane/EtOAc 2:1);

¹H NMR (300 MHz, CDCl₃) δ 0.85 (t, 3H, J=6.7 Hz), 1.08 (d, 3H, J=6.9 Hz), 1.20–1.30 (m, 26H), 1.35–1.45 (m, 2H), 2.20 (br s, 1H), 3.72–3.82 (m, 1H) 4.45–4.60 (m, 1H), 6.58 (d, 1H, J=8.6 Hz), 7.18–7.38 (m, 5H), 8.39 (br s, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 12.9, 14.0, 22.6, 25.8, 29.2, 29.4, 29.5, 29.5, 29.6, 31.8, 33.7, 54.5, 73.5, 124.4, 126.6, 129.9, 136.4, 179.0;

ESMS calcd for C₂₅H₄₃N₂OS (M−H) 419.3, found 419.2.

Example 108 (2S,3R)-2-Amino-N-(phenylcarbamoyl)-3-octadecanol, 110

According to the method of Example 107, from aminoalcohol 1 (23 mg, 0.08 mmol) and PhNCO (18 μL, 0.16. mmol), phenylurea 110 was obtained as a white solid (15 mg, 46% yield).

R_(f) 0.50 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.7 Hz), 1.11 (d, 3H, J=6.9 Hz), 1.20–1.30 (m, 26H), 1.35–1.45 (m, 2H), 2.17 (br s, 1H), 3.63–3.73 (m, 1H) 3.90–4.06 (m, 1H), 5.02 (d, 1H, J=7.2 Hz), 6.58 (br s, 1H), 7.05–7.12 (m, 1H), 7.25–7.34 (m, 4H);

ESMS calcd for C₂₅H₄₅N₂O₂ (M+H) 405.3, found 405.4.

Example 109 (2S,3R)-2-Amino-N-(n-butylcarbamoyl)-3-octadecanol, 111

According to the method of Example 107, from aminoalcohol 1 (27 mg, 0.09 mmol) and n-BuNCO (21 μL, 0.19 mmol), n-butylurea 111 was obtained as a white solid (13 mg, 36% yield).

R_(f) 0.25 (hexane/EtOAc 2:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.9 Hz), 0.92.(t, 3H, J=7.2 Hz), 1.08 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 28H), 1.40–1.55 (m, 4H), 2.91 (br s, 1H), 3.14 (q, 2H, J=6.5 Hz), 3.61 (br s, 1H), 3.78–3.88 (m, 1H), 4.56–4.66 (m, 2H);

ESMS calcd for C₂₃H₄₉N₂O₂ (M+H) 385.4, found 385.4.

Example 110 (2S,3R)-2-(Methanesulfonamide)-3-octadecanol, 112

To a solution of aminoalcohol 1 (40 mg, 0.14 mmol) in CH₂Cl₂ (5.0 mL) at room temperature, ClSO₂Me (11 μL, 0.14 mmol) was added. After stirring for 1 h, the reaction was quenched with H₂O (10 mL), extracted with CH₂Cl₂ (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 4:1) to obtain sulfonamide 112 as a white solid (49 mg, 96% yield).

R_(f) 0.13 (hexane/EtOAc 4:1);

¹H NMR (300 MHz, CD₃OD) δ 0.85 (t, 3H, J=6.8 Hz), 1.19 (t, 3H J=6.8 Hz), 1.20–1.40 (m, 26H), 1.47–1.53 (m, 2H), 1.86 (d, 1H,. J=5.1 Hz), 3.00 (s, 3H), 3.53 (t, 1H, J=6.1 Hz), 3.66–3.72 (m, 1H), 4.66 (d, 1H, J=8.1 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 12.0, 14.5, 16.4, 23.2, 26.9, 27.2, 30.6, 30.7, 30.8, 33.1, 34.2, 41.6, 55.3, 71.5;

ESMS calcd for C₁₈H₃₈NO (M−SO₂Me) 286.2, found 286.5.

Example 111 (2S,3R)-2-(Methanesulfonamide)-3-nonadecanol, 113

According to the method of Example 110, from aminoalcohol 2 (25 mg, 0.08 mmol), sulfonamide 113 was obtained as a white solid (29 mg, 94% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.87 (t, 3H, J=6.4 Hz), 1.17 (d, 3H, J=6.4 Hz), 1.20–1.40 (m, 28H), 1.46–1.53 (m, 2H), 1.98–2.05 (m, 1H), 2.97–3.03 (m, 1H), 3.47–3.58 (m, 1H), 3.68–3.74 (m, 1H), 4.77–4.83 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.3, 15.5, 22.9, 26.2, 29.5, 29.7, 29.8, 29.9, 32.1, 33.4, 42.0, 54.0, 74.6;

ESMS calcd for C₁₉H₄₀NO (M−SO₂Me) 300.3, found 300.3.

Example 112 (2S,3R)-2-(2,2,2-Trifluoroacetylamino)-3-octadecanol, 114, and (2S,3R)-2-(2,2,2-trifluoroacetylamino)-O-(2,2,2-trifluoroacetyl)-octadecanol, 115

To a solution of aminoalcohol 1 (27 mg, 0.09 mmol) in CH₂Cl₂ (5.0 mL) at room temperature, trifluoroacetic anhydride (12.8 μL, 0.09 mmol) was added. After stirring for 1 h, the solvents were removed in vacuo. The crude was purified by column chromatography on silica (hexane/CH₂Cl₂ 1:1) to obtain 114 (9 mg, 25% yield) R_(f) 0.34 (hexane/CH₂Cl₂ 1:1) and 115 (11 mg, 24% yield) R_(f) 0.52 (hexane/CH₂Cl₂ 1:1) as white solids.

114: ¹H NMR (300 MHz, CD₃OD) δ 0.85 (t, 3H, J=6.9 Hz), 1.05 (d, 3H, J=7.0 Hz), 1.19–1.38 (m, 26H), 1.45–1.53 (m, 2H), 3.60–3.66 (m, 1H), 3.93–3.98 (m, 1H), 6.65 (d, 1H, J=7.5 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 12.9, 14.3, 15.4, 22.9, 25.9, 29.5, 29.7, 29.8, 31,8, 32.1, 34.2, 49.6, 73.2, 76.8, 114.4, 118.2, 121.8, 151.4, 156.9;

ESMS calcd for C₂₀H₃₈F₃NO₂Na (M+Na) 404.3, found 404.8.

115: ¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=7.6 Hz), 1.20–1.39 (m, 26H), 2.46–2.55 (m, 2H), 4.01–4.43 (m,1H), 4.95–5.24 (m, 1H), 6.00–6.34 (m, 1H).

Example 113 (2S,3R)-2-(2,2,2-Trifluoroacetylamino)-3-nonadecanol, 116, and (2S,3R)-2-(2,2,2-trifluoroacetylamino)-O-(2,2,2-trifluoroacetyl)-nonadecanol, 117

According to the method of Example 112, from aminoalcohol 2 (22 mg, 0.07 mmol), 116 (6 mg, 22% yield) and 117 (8 mg, 23% yield) were obtained as white solids.

116: ¹H NMR (300 MHz, CD₃OD) δ 0.85 (t, 3H, J=6.8 Hz), 1.01 (d, 3H, J=6.8 Hz), 1.23–1.41 (m, 28H), 1.45–1.53 (m, 2H), 3.65–3.73 (m, 1H), 3.96–4.06 (m, 1H), 6.68–6.73 (m, 1H).

117: ¹H NMR (300 MHz, CD₃OD) δ 0.88 (t, 3H, J=7.6 Hz,), 1.25–1.38 (m, 26H), 2.47–2.60 (m, 2H), 4.00–4.40 (m, 1H), 4.97–5.28 (m, 1H), 6.01–6.35 (m, 1H).

Example 114 (2S,3R)-2-Amino-N-(trans-cinnamoyl)-3-octadecanol, 118

To a solution of aminoalcohol 1 (30 mg, 0.10 mmol) in CH₂Cl₂ (3.0 mL) at room temperature, pyridine (58 mL, 0.11 mmol) and cinnamoyl chloride (16.6 mg, 0.36 mmol) were added. After stirring for 1 h, the reaction was quenched with H₂O (10 mL), extracted with CH₂Cl₂ (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 4:1) to obtain 118 as a white solid (32 mg, 74% yield).

R_(f) 0.31(hexane/EtOAc 2:1);

¹H NMR (300 MHz, CD₃OD) δ 0.87 (t, 3H, J=6.9 Hz), 1.16 (d, 3H, J=6.9 Hz), 1.21–1.40 (m, 26H), 1.33–1.40 (m, 2H), 2.28–2.35 (m, 1H), 3.64–3.71 (m, 1H), 4.06–4.18 (m, 1H), 5.92 (d, 1H, J=15.6 Hz), 6.40 (d, 1H, J=15.6 Hz), 7.31–7.36 (m, 3H), 7.41–7.50 (m, 2H), 7.62 (d, 1H, J=15.6 Hz);

¹³C NMR (75 MHz, CDCl3) δ 14.9, 25.3, 26.2, 29.5, 29.9, 33.8, 49.9, 74.3, 124.2, 126.8, 129.8, 130.9, 136.1, 165.1;

ESMS calcd for C₂₇H₄₅NO₂Na (M+Na) 438.3, found 438.3.

Example 115 (2S,3R)-2-Amino-N-[trans-3-(trifluoromethyl)-cinnamoyl]-3-octadecanol, 119

According to the method of Example 114, from aminoalcohol 1 (30 mg, 0.10 mmol) and 3-(trifluoromethyl)-cinnamoyl chloride (24.6 mg, 0.10 mmol), amide 119 was obtained as a white solid (28 mg, 56% yield).

R_(f) 0.30 (hexane/EtOAc 2:1);

¹H NMR (300 MHz, CD₃OD) δ 0.87 (t, 3H, J=6.9 Hz), 1.16 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 26H), 1.35–1.41 (m, 2H), 3.68–3.74 (m, 1H), 3.98–4.20 (m, 1H), 6.06 (d, 1H, J=9.6 Hz), 6.45 (d, J=6.9 Hz, 1H), 7.48–7.78 (m, 4H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 22.9 26.2, 29.6, 29.8, 29.9, 32.1, 33.9, 49.9, 74.4, 122.8, 124.1, 124.2, 126.3, 129.5, 131.3, 135.8, 139.7, 165.2;

ESMS calcd for C₂₈H₄₄F₃NO₂Na (M+Na) 506.3, found 506.4.

Example 116 (2S,3R)-2-Amino-N-(palmitoyl)-3-octadecanol, 120

To a solution of aminoalcohol 1 (30 mg, 0.10 mmol) in CH₂Cl₂ (3.0 mL) at room temperature, palmitic acid (28 mg, 0.11 mmol), EDC (50.2 mg, 0.26 mmol), DIPEA (39 μL, 0.15 mmol) and DMAP (1.2 mg, 0.01 mmol) were added. After stirring for 2 h, the reaction was quenched with H₂O (10 mL), extracted with CH₂Cl₂ (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 4:1) to obtain 120 as a white solid (48 mg, 87% yield).

R_(f) 0.21 (hexane/EtOAc 4:1);

¹H NMR (300 MHz, CD₃OD) δ 0.85–0.94 (m, 6H), 1.08 (d, 3H, J=7.1 Hz), 1.20–1.40 (m, 52H), 1.58–1.65 (m, 2H) 2.16 (t, 2H, J=7.1Hz), 2.29–2.33 (m, 1H), 3.58–3.64 (m, 1H), 3.93–4.13 (m, 1H), 5.72 (d, 1H, J=7.1 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 15.2, 22.7, 25.8, 25.9, 29.2, 29.3, 29.5, 29.6, 29.7, 31.9, 33.5, 36.9, 49.4, 65.8, 74.4, 173.1;

ESMS calcd for C₃₄H₆₉NO₂Na (M+Na) 546.5, found 546.8.

Example 117 (2 S,3R)-2-[2-(tert-Butoxycarbonylaminio)-3-methylbutyramide)]-3-octadecanol, 121

To a solution of aminoalcohol 1 (30 mg, 0.10 mmol) in CH₂C1₂ (3.0 mL) at room temperature, N-Boc-valine (23 mg, 0.11 mmol), EDC (50.2 mg, 0.26 mmol), DIPEA (39 μL, 0.15 mmol) and DMAP (1.2 mg, 0.01 mmol) were added. After stirring for 2 h, the reaction was quenched with H₂O (10 mL), extracted with CH₂Cl₂ (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 4:1) to obtain 121 as a white solid (48 mg, 87% yield).

R_(f) 0.13 (hexane/EtOAc 4:1);

¹H NMR (300 MHz, CD₃OD) δ 0.86 (t, 3H, J=6.9 Hz), 0.91 (d, 3H, J=6.9 Hz), 0.96 (d, 3H, J=6.9 Hz), 1.08 (d, 3H, J=6.9 Hz), 1.20–1.40 (m, 26H), 1.38–1.46 (m, 11H), 1.99–2.23 (m, 1H), 2.33–2.78 (m, 1H), 3.64 (m, 1H), 3.83 (t, 1H, J=6.3 Hz), 3.98 (m, 1H), 5.06 (d, 1H, J=6.8 Hz), 6.29 (d, 1H, J=7.8 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 13.7, 14.1, 17.8, 19.3, 22.7,.26.0, 28.3, 29.3, 29.5, 29.7, 30.6, 31.9, 33.5, 49.6, 60.4, 73.8, 157.4, 171.3;

ESMS calcd for C₂₈H₅₇N₂O₄ (M+Ha) 485.4, found 485.7.

Example 118 (2S,3R)-2-[2-Amino-3-methylbutyramide)]-3-octadecanol hydrochloride, 122

According to the method of Example 95, from N-Boc derivative 121 (24 mg, 0.05 mmol), hydrochloride 122 was obtained as a white solid (15 mg, 75% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.87 (t, 3H, J=6.8 Hz), 1.07–1.11 (m, 6H), 1.13 (d, 3H, J=6.8 Hz), 1.21–1.40 (m, 26H), 1.41–1.52 (m, 2H), 2.09–2.11 (m, 1H), 3.40–3.47 (m, 1H), 3.66–3.77 (m, 1H), 3.87–3.93 (m, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 12.7, 13.1, 16.7, 17.8, 18.3, 21.6, 25.2, 27.2, 28.3, 28.7, 29.6, 30.9, 32.3, 49.6, 66.0,. 72.5, 166.7;

ESMS calcd for C₂₃H₄₉N₂O₂ (M−Cl) 385.3, found 385.3.

Example 119 (2S)-2-(N-tert-Butoxycarbonylamino)-3-heptadecanone, 123

To a solution of aminoalcohol 37 (82 mg, 0.274 mmol) in dioxane (0.7 mL) and H₂O (0.4 mL) at room temperature, NaOH (1M, aq., 0.3 mL) was added followed by Boc2O (66 mg, 0.301 mmol). After stirring for 2 h, the reaction was diluted with EtOAc (10 mL) and KHSO₄ (10% aq., 10 mL) was added. The layers were separated and the aqueous layer extracted with EtOAc (3×10 mL). The organic layers were dried over Na₂SO₄ and concentrated in vacuo to obtain the crude N-Boc derivative as a white solid. To a cold (−78° C.) solution of (COCl)₂ (2M in CH₂Cl₂, 0.22 mL, 0.447 mmol) in CH₂Cl₂ (4.5 mL), DMSO (0.063 mL, 0.894 mmol) was added dropwise. After stirring at −78° C. for 15 min, a solution of the N-Boc derivative (69 mg, 0.179 mmol) in CH₂Cl₂ (2 mL) was added dropwise. The mixture was stirred at −78° C. for 1 h, and then Et₃N (0.187 mL, 1.34 mmol) was added. The reaction was warmed up to 0° C. and stirred for 15 min, followed by the addition of NH₄Cl (15 mL, sat. aq.). The crude was extracted with CH₂Cl₂ (3×15 mL), washed successively with NaHCO₃ (30 mL, sat. aq.) and brine (30 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 5:1) to obtain ketone 123 as a white solid (40 mg, 56% yield) together with unreacted starting material (30 mg). R_(f) 0.42 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.85 (t, 3H, J=6.4 Hz), 1.20–1.37 (m, 25H), 1.42 (s, 9H), 1.54–1.62 (m, 2H), 2.38–2.56 (m, 2H), 4.29 (quint, 1H, J=6.5 Hz), 5.28 (br d, 1H, J=5.2 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.0, 17.9, 22.6, 23.5, 28.3, 29.2, 29.3, 29.4, 29.5, 29.6, 31.9, 39.1, 55.0, 209.7;

ESMS calcd for C₂₂H₄₃NO₃Na (M+Na) 392.3, found 392.3.

Example 120 (2S)-2-Amino-3-heptadecanone hydrochloride, 124

According to the method of Example 95, from ketone 123 (33.5 mg, 0.091 mmol), hydrochloride 124 was obtained as a white solid (22 mg, 79% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.9 Hz), 1.20–1.35 (m, 22H), 1.51 (d, 3H, J=7.4 Hz), 1.55–1.65. (m, 2H), 2.50–2.72 (m, 2H), 4.13 (q, 1H, J=7.4 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.4, 15.7, 23.7, 24.3, 30.1, 30.5, 30.5, 30.6, 30.7, 30.8, 33.1, 39.2, 55.8, 207.4;

ESMS calcd for C₁₇H₃₆NO (M−Cl) 270.3, found 270.2.

Example 121 (2S)-2-(N-tert-Butoxycarbonylamino)-3-octadecanone, 125

According to the method of Example 119, from aminoalcohol 1 (53 mg, 0.186 mmol), ketone 125 was obtained as a white solid (27 mg, 38% yield), together with unreacted starting alcohol (24 mg). R_(f) 0.42 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.4 Hz), 1.20–1.37 (m, 27H), 1.43 (s, 9H), 1.54–1.62 (m, 2H), 2.38–2.56 (m, 2H), 4.30 (quint, 1H, J=6.8 Hz), 5.27. (br s, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 17.9, 22.7, 23.6, 28.3, 29.2, 29.3, 29.4, 29.6, 29.7, 31.9, 39.2, 55.0, 209.7;

ESMS calcd for C₂₃H₄₅NO₃Na (M+Na) 406.3, found 406.3.

Example 122 (2S)-2-Amino-3-octadecanone hydrochloride, 126

According to the method of Example 95, from ketone 125 (24 mg, 0.063 mmol), hydrochloride 126 was obtained as a white solid (17 mg, 85% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.9 Hz), 1.20–1.35 (m, 24H), 1.51 (d, 3H, J=7.4 Hz), 1.55–1.65 (m, 2H), 2.50–2.72 (m, 2H), 4.13 (q, 1H, J=7.4 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.4, 15.7, 23.7, 24.3, 30.1, 30.5, 30.5, 30.6, 30.8, 33.1, 39.2, 55.8, 207.4;

ESMS calcd for C₁₈H₃₈NO (M−Cl) 284.3, found 284.3.

Example 123 (2S)-2-Amino-3-octadecanoneoxime, 127

To a solution of ketone 126 (108 mg, 0.34 mmol) in 2.5 mL of EtOH, NH₂OH.HCl (117 mg, 1.69 mmol) and AcONa (249 mg, 3.04 mmol) were added. The mixture was stirred at 80° C. for 8 h, and then the solvent was evaporated in vacuo. The residue was suspended in H₂O, filtered and washed with H₂O. The collected solid was recyrstallised from EtOAc to obtain oxime 127 as a white solid (70 mg, 69% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.7 Hz), 1.20–1.35 (m, 27H), 1.55–1.65 (m, 2H), 2.18 (ddd, 1H, J=12.9, 10.1, 6.0 Hz), 2.47 (ddd, 1H, J=12.9, 9.6, 6.4 Hz), 3.72 (q, 1H, J=6.7 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.5, 18.3, 23.7, 24.0, 26.6, 26.7, 30.4, 30.5,30.7, 30.8, 31.0, 33.1, 50.2, 158.0;

ESMS calcd for C₁₈H₃₉N₂O (M+H) 299.3, found 299.3.

Example 124 (2S)-2-(N-tert-Butoxycarbonylamino)-3-nonadecanone, 128

According to the method of Example 119, from aminoalcohol 2 (59 mg, 0.197 mmol), ketone 128 was obtained as a white solid (44 mg, 56% yield).

R_(f) 0.42 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.85 (t, 3H, J=6.4 Hz), 1.20–1.37 (m, 29H), 1.42 (s, 9H), 1.54–1.62 (m, 2H), 2.38–2.56 (m, 2H), 4.28 (quint, 1H, J=6.7 Hz), 5.29 (br d, 1H, J=6.2 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.0, 17.8, 22.6, 23.5, 28.3, 29.2, 29.3, 29.4, 29.5, 29.6, 31.9, 39.1, 55.0, 209.7;

ESMS calcd for C₂₄H₄₇NO₃Na (M+Na) 420.4, found 420.2.

Example 125 (2S)-2-Amino-3-nonadecanone hydrochloride, 129

According to the method of Example 95, from ketone 128 (33 mg, 0.083 mmol), hydrochloride 129 was obtained as a white solid (25 mg, 90% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.9 Hz), 1.20–1.35 (m, 26H), 1.51 (d, 3H, J=7.4 Hz), 1.55–1.65 (m, 2H), 2.50–2.72 (m, 2H), 4.13 (q, 1H, J=7.4 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.4, 15.7, 23.7, 24.3, 30.1, 30.5, 30.5, 30.6, 30.8, 33.1, 39.2, 55.8, 207.4;

ESMS calcd for C₁₉H₄₀NO (M−Cl) 298.3, found 298.3.

Example 126 (2S)-2-(N-tert-Butoxycarbonylamin)-3-eicosadecanone, 130

According to the method of Example 119, from aminoalcohol 3 (81 mg, 0.258 mmol), ketone 130 was obtained as a white solid (75 mg, 70% yield).

R_(f) 0.42 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.86 (t, 3H, J=6.2 Hz), 1.20–1.37 (m, 31H), 1.42 (s, 9H), 1.54–1.62 (m, 2H), 2.38–2.56 (m, 2H), 4.29 (quint, 1H, J=6.5 Hz), 5.29 (br d, 1H, J=5.4 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.0, 17.8, 22.6, 23.5, 28.3, 29.2, 29.3, 29.4, 29.5, 29.6, 31.9, 39.1, 55.0, 209.6;

ESMS calcd for C₂₅H₄₉NO₃Na (M+Na) 434.4, found 434.3.

Example 127 (2 S)-2-Amino-3-eicosadecanone hydrochloride, 131

According to the method of Example 95, from ketone 130 (47 mg, 0.114 mmol), hydrochloride 131 was obtained as a white solid (30.5 mg, 77% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.9 Hz), 1.20–1.35 (m, 28H), 1.50 (d, 3H, J=7.2 Hz), 1.55–1.65 (m, 2H), 2.50–2.72 (m, 2H), 4.13 (q, 1H, J=7.2 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.4, 15.7, 23.7, 24.3, 30.1, 30.5, 30.5, 30.6, 30.7, 30.8, 33.1, 39.2, 55.8, 207.4;

ESMS calcd for C₂₀H₄₂NO (M−Cl) 312.3, found 312.3.

Example 128 (3S)-3-(N-tert-Butoxycarbonylamino)-4-nonadecanone, 132

According to the method of Example 119, from aminoalcohol 57 (82 mg, 0.274 mmol), ketone 132 was obtained as a white solid (54 mg, 50% yield).

R_(f) 0.42 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.86 (t, 6H, J=7.0 Hz), 1.20–1.35 (m, 24H), 1.43 (s, 9H), 1.55–1.65 (m, 3H), 1.84–1.96 (m, 1H), 2.38–2.56 (m, 2H), 4.28 (q, 1H, J=5.5 Hz), 5.24 (br d, 1H, J=6.9 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 9.2, 14.0, 22.6, 23.5, 24.8, 28.3, 29.2, 29.3, 29.4, 29.6, 29.6, 31.9, 39.8, 60.1, 209.4;

ESMS calcd for C₂₄H₄₇NO₃Na (M+Na) 420.4, found 420.3.

Example 129 (3S)-3-Amino-4-nonadecanone hydrochloride, 133

According to the method of Example 95, from ketone 132 (36.5 mg, 0.092 mmol), hydrochloride 133 was obtained as a white solid (29 mg, 95% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.7 Hz), 1.00 (t, 3H, J=7.5 Hz), 1.20–1.35 (m, 24H), 1.55–1.65 (m, 2H), 1.82–1.96 (m, 1H), 2.00–2.12 (m, 1H), 2.50–2.72 (m, 2H), 4.11 (dd, 1H, J=7.2, 4.5 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 9.3, 14.5, 23.8, 23.9, 24.3, 30.1, 30.5, 30.5, 30.6, 30.7, 30.8, 33.1, 39.8, 61.0, 207.1;

ESMS calcd for C₁₉H₄₀NO (M−Cl) 298.3, found 298.3.

Example 130 (2R)-2-(N-tert-Butoxycarbonylamino)-3-octadecanone, 134

According to the method of Example 119, from aminoalcohol 81 (53 mg, 0.186 mmol), ketone 134 was obtained as a white solid (40 mg, 56% yield).

R_(f) 0.42 (hexane/EtOAc 5:1);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.4 Hz), 1.20–1.37 (m, 27H), 1.43 (s, 9H), 1.54–1.62 (m, 2H), 2.38–2.56 (m, 2H), 4.30 (quint, 1H, J=6.8 Hz), 5.27 (br s, 1H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 17.9,.22.7, 23.6, 28.3, 29.2, 29.3, 29.4, 29.6, 29.7, 31.9, 39.2, 55.0, 209.7;

ESMS calcd for C₂₃H₄₅NO₃Na (M+Na) 406.3, found 406.2.

Example 131 (2R)-2-Amino-3-octadecanone hydrochloride, 135

According to the method of Example 95, from ketone 134 (30 mg, 0.078 mmol), hydrochloride 135 was obtained as a white solid (24 mg, 96% yield).

¹H NMR (300 MHz, CD₃OD) δ 0.89 (t, 3H, J=6.9 Hz), 1.20–1.35 (m, 24H), 1.51 (d, 3H, J=7.4 Hz), 1.55–1.65 (m, 2H), 2.50–2.72 (m, 2H), 4.13 (q, 1H, J=7.4 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.4, 15.7, 23.7, 24.3, 30.1, 30.5, 30.5, 30.6, 30.8, 33.1, 39.2, 55.8, 207.4;

ESMS calcd for C₁₈H₃₈NO (M−Cl) 284.3, found 284.2.

Example 132 (2S,3R)-2-Amino-1-(tert-butyldiphenylsilyloxy)-octadec4-en-3-ol, 136

To a solution of D-erythro-sphingosine (46 mg, 0.153 mmol) in CH₂Cl₂ (1.5 mL) at room temperature, Et₃N (32 μL, 0.230 mmol), TBDPSCl (44 μL, 0.169 mmol) and 4-DMAP (ca. 5 mg, cat.) were added. After stirring for 4 h, the reaction was quenched with H₂O (10 mL), extracted with EtOAc (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 5:1 to 100% EtOAc) to obtain 136 as a colorless oil (33 mg, 40% yield).

R_(f) 0.20 (hexane/EtOAc 1:5);

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=6.9 Hz), 1.06 (s, 9H), 1.20–1.40 (m, 22H), 1.91 (br s, 3H), 2.01 (q, 2H, J=6.5 Hz), 2.93 (q, 1H, J=5.5 Hz), 3.69 (d, 2H, J=4.5 Hz), 4.09 (t, 1H, J=6.1 Hz), 5.40 (dd, 1H, J=15.3, 6.9 Hz), 5.73 (dt, 1H, J=15.4, 6.5 Hz), 7.35–7.46 (m, 6H), 7.64–7.68 (m, 4H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 19.2, 22.7, 26.8, 29.2, 29.2, 29.3, 29.5, 29.6, 29.7, 31.9, 32.3, 56.3, 66.2, 74.6, 127.7, 128.9, 129.8, 133.1, 134.1, 135.5;

ESMS calcd for C₃₄H₅₆NO₂Si (M+H) 538.4, found 538.4.

Example 133 (4S,5R)-4-(tert-Butyldimethylsilyloxymethyl)-5-(n-pentadec-2′-enyl)-1,3-oxazolidinone, 137

According to the method of Example 105, from aminoalcohol 136 (33 mg, 0.061 mmol), oxazolidinone 137 was obtained as a colorless oil (32 mg, 92% yield).

R_(f) 0.60 hexane/EtOAc 1:1);

¹H NMR (300 MHz, CDCl₃) δ 0.86 (t, 3H, J=7.0 Hz), 1.06 (s. 9H), 1.20–1.40 (m, 22H), 2.00 (q, 2H, J=6.9 Hz), 3.58 (dd, 1H, J=10.6, 4.7 Hz), 3.64 (dd, 1H, J=10.6, 6.7 Hz), 3.82–3.88 (m, 1H), 5.02 (t, 1H, J=8.1 Hz), 5.32 (br s, 1H), 5.51 (dd, 1H, J=15.4, 8.1 Hz), 5.83 (dt, 1H, J=15.4, 6.5 Hz), 7.37–7.46 (m, 6H), 7.61–7.65 (m, 4H);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 19.1, 22.7, 26.7, 28.7, 29.1, 29.3, 29.4, 29.5, 29.6, 31.9, 32.1, 57.2, 63.1, 79.4, 122.1, 127.9, 130.0, 132.7, 135.5, 138.4, 158.9;

ESMS calcd for C₃₅H₅₃NO₃SiNa (M+Na) 586.4, found 586.5.

Example 134 (4S,5R)-4-(Hydroxymethyl)-5-(n-pentadec-2′-enyl)-1,3-oxazolidinone, 138

To a solution of 137 (32 mg, 0.057 mmol) in THF (0.6 mL) at room temperature, TBAF (1M in THF, 113 μL, 0.113 mmol) was added. After stirring for 30 min, the reaction was quenched with H₂O (10 mL), extracted with EtOAc (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 1:1 to 1:5) to obtain alcohol 138 as a white solid (13 mg, 70% yield).

R_(f) 0.27 (hexane/EtOAc 1:5);

¹H NMR (300 MHz, CD₃OD) δ 0.90 (t, 3H, J=6.7 Hz), 1.25–1.50 (m, 22H), 2.12 (q, 2H, J=6.9 Hz), 3.51 (dd, 1H, J=11.6, 5.9 Hz), 3.58 (dd, 1H, J=11.6, 4.0 Hz), 3.84 (ddd, 1H, J=8.4, 5.9, 4.2 Hz), 5.10 (t, 1H, J=8.2 Hz), 5.67 (dd, 1H, J=15.4, 8.2 Hz), 5.90 (dt, 1H,. J=15.4, 6.7 Hz);

¹³C NMR (75 MHz, CD₃OD) δ 14.5, 23.8, 30.0, 30.2, 30.5, 30.6, 30.8, 33.1, 33.3, 58.7, 62.2, 81.5, 124.4, 139.1, 168.1;

ESMS calcd for C₁₉H₃₅NO₃Na (M+Na) 348.3, found 348.2.

Example 135 (4S,5R)-4-(Fluoromethyl)-5-(n-pentadec-2′-enyl)-1,3-oxazolidinone, 139

To a cold (−78° C.) solution of 138 (11.5 mg, 0.035 mmol) in THF (0.35 mL), DAST (14 μL, 0.106 mmol) was added. After stirring for 30 min, the mixture was warmed up to room temperature and stirred for 2 h. The reaction was quenched with NaHCO₃ (5 mL), extracted with EtOAc (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography, on silica (hexane/EtOAc 1:1) to obtain fluoride 139 as a white solid (7.5 mg, 65% yield).

R_(f) 0.22 (hexane/EtOAc 1:1);

¹H NMR (300 MHz, CDCl₃) δ 0.88 (t, 3H, J=7.0 Hz), 1.20–1.40 (m, 22H), 2.09 (q, 2H, J=6.9 Hz), 4.03–4.13 (m, 1H), 4.41 (dm, 2H, J=46.5 Hz), 5.11 (t, 1H, J=7.9 Hz), 5.44 (br s, 1H), 5.48 (dd, 1H, J=15.3, 8.1 Hz), 5.95 (dt, 1H, J=15.3, 7.0 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 22.6, 28.6, 29.1, 29.3, 29.4, 29.5, 29.6, 31.9, 32.2, 55.3 (d), 79.0 (d), 81.8 (d), 121.4, 139.4, 159.3;

ESMS calcd for C₁₉H₃₄FNO₂Na (M+Na) 350.3, found 350.2.

Example 136 (2S,3R)-2-Amino-1-fluoro-octadec-4-en-3-ol, 140

To a solution of 139 (46 mg, 0.140 mmol) in dioxane (2.5 mL), NaOH (1M, 1.40 mL, 1.405 mmol) was added. After stirring for 4 h at 100° C., the reaction was quenched with H₂O (10 mL), extracted with EtOAc (3×10 mL), dried over Na₂SO₄ and concentrated in vacuo. The crude was purified by column chromatography on silica (hexane/EtOAc 1:1 to 100% EtOAc) to obtain aminoalcohol 140 as a white solid (20 mg, 47% yield).

R_(f) 0.18 (hexane/EtOAc 1:5);

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.2 Hz), 1.20–1.40 (m, 22H), 1.79 (br s, 3H), 2.05 (q, 2H, J=6.9 Hz), 3.03–3.13 (m, 1H), 4.05 (t, 1H, J=6.4 Hz), 4.40 (ddd, 1H, J=47.5, 9.2, 6.9 Hz), 4.51 (ddd, 1H, J=47.0, 9.2, 4.2 Hz), 5.44 (dd, 1H, J=15.6, 7.4 Hz), 5.76 (dt, 1H, J=15.4, 6.9 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 22.7, 29.1, 29.2, 29.3, 29.4, 29.6, 29.6, 31.9, 32.3, 55.2 (d), 73.1 (d), 85.2 (d), 128.4, 135.2;

ESMS calcd for C₁₈H₃₇FNO (M+H) 302.3, found 302.2.

Example 137 (2S,3R)-2-Amino-1-fluoro-3-octadecanol, 141

According to the method of Example 89, from olefin 140 (4 mg, 0.013 mmol), aminoalcohol 141 was obtained as a white solid (1.8 mg, 45% yield).

¹H NMR (300 MHz, CDCl₃) δ 0.87 (t, 3H, J=6.7 Hz), 1.20–1.40 (m, 26H), 1.50–1.60 (m, 2H), 1.87 (br s, 3H), 3.04–3.14 (m, 1H), 3.54–3.62 (m, 1H), 4.40 (ddd, 1H, J=48.0, 9.2, 7.4 Hz), 4.56 (ddd, 1H, J=46.8, 9.2, 3.9 Hz);

¹³C NMR (75 MHz, CDCl₃) δ 14.1, 22.7, 26.0, 29.3, 29.6, 29.7, 31.9, 32.9, 55.0 (d), 72.5 (d), 85.1 (d);

ESMS calcd for C₁₈H₃₉FNO (M+H) 304.3, found 304.3. 

1. A compound of formula:

wherein: the terminal group —C(X)₃ is CH₃; Y is OR₁, wherein R₁ is selected from H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, or substituted or unsubstituted aryl and wherein the dotted line indicates an optional double bond such that Y can also be ═O; or the group Y with NR₂R₃ and the intervening atoms can form a heterocycle; the terminal group —C(Z)₃ is CH₃; z is 11 to 19; y is 1 to 3, wherein when y is 2, then z is not 14; R₂ and R₃ are the same or different and each is H, C(═O)R′, C(═S)R′, P(═O)R′R″, S(═O)R′R″, S(═O)₂R′, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl; each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, NHR′, NR′R″, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₁–C₁₈ alkoxy, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl; and salts thereof.
 2. A compound or salt according to claim 1, wherein Y is OH, O(C═O)R′ where R′ is optionally halogen-substituted alkyl, OP(═O)R′₂ where R′ is alkoxy, NH₂, ═O, ═NOH, or the group Y when OH with NR₂ R₃ and the intervening atoms form a heterocycle of formula:


3. A compound or salt according to claim 1, wherein R₂ and R₃ are the same.
 4. A compound or salt according to claim 1, wherein at least one of R₂ and R₃ is alkyl; alkyl substituted by aryl; hydrogen; C (═O)R′ where R′ is alkyl or alkoxy, halogen-substituted alkyl, optionally substituted amino-substitued alkyl; aryloxy, alkoxy, optionally substituted aryl-substituted alkenyl; (C═S)NHR′ where R′ is aryl; (C═O)NHR′ where R′ is aryl or alkyl; SO₂R′ where R′ is alkyl, or (C═O)R′ where R′ is optionally substituted aminoalkyl thereby giving an optionally substituted aminoacid acyl group.
 5. A compound or salt according to claim 1, which has the stereochemistry


6. A compound or salt according to claim 1, wherein two or more of the following criteria are met: Y is OR₁ where R₁ is H, methyl, acetyl, PO(OMe)₂, or COCF₃; or Y is ═O; R₂ and R₃ are independently selected from the group consisting of H, methyl, acetyl, benzyl, Boc, CSNHPh, CONHPh, CONH^(n)Bu, SO₂Me, COCF₃, COCH═CHPh, COCH═CHPhCF₃, COC₁₅H₃₂, COCH(NHBoc)CHMe₂, COCH(NH₃ ⁺Cl⁻)CHMe₂; the stereochemistry is

or the compound or salt is in the form of a salt.
 7. A compound or salt according to claim 6, which meets one of the following criteria: z is not 12, 13 or 14; or Y is not OH; or At least one of R₂ and R₃ is not hydrogen; the compound or salt is in the form of a salt.
 8. A compound or salt according to claim 1, which is of the formula:

where z is 11 to 19; Y is OR₁ where R₁ is H, methyl, acetyl, PO(OMe)₂, or COCF₃; or Y is ═O; R₂ and R₃ are independently selected from the group consisting of H, methyl, acetyl, benzyl, Boc, CSNHPh, CONHPh, CONHnBu, SO₂Me, COCF₃, COCH═CHPh, COCH═CHPhCF₃, COC₁₅H₃₂, COCH(NHBoc)CHMe₂, COCH (NH₃ ⁺Cl⁻)CHMe₂; Z represents methyl or ethyl.
 9. A compound or salt according to claim 1, which is one of the following compounds:


10. A pharmaceutical composition comprising a compound of formula:

wherein: the terminal group —C(X)₃ is —CH₃; Y is OR₁, wherein R₁ is selected from H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, or substituted or unsubstituted aryl and wherein the dotted line indicates an optional double bond such that Y can also be ═O; or the group Y with NR₂R₃ and the intervening atoms can form a heterocycle; the terminal group —C(Z)₃ is CH₃; z is 10 to 19; y is 1 to 3; R₂ and R₃ are the same or different and each is H, C(═O)R′, C(═S)R′, P(═O)R′R″, S(═O)R′R″, S(═O)₂R′, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl; each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, NHR′, NR′R″, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₁–C₁₈ alkoxy, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl; and salts thereof, together with a pharmaceutically acceptable carrier.
 11. A method of treating a tumor which includes administration of an effective amount of a compound of formula:

wherein: the terminal group —C(X)₃ is —CH₃; Y is OR₁, wherein R₁ is selected from H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, or substituted or unsubstituted aryl and wherein the dotted line indicates an optional double bond such that Y can also be ═O; or the group Y with NR₂R₃ and the intervening atoms can form a heterocycle; the terminal group —C(Z)₃ is CH₃; z is 10 to 19; y is 1 to 3; R₂ and R₃ are the same or different and each is H, C(═O)R′, C(═S)R′, P(═O)R′R″, S(═O)R′R″, S(═O)₂R′, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl; each of the R′, R″ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, NHR′, NR′R″, SH, CN, halogen, ═O, C(═O)H, C(═O)CH₃, CO₂H, CO₂CH₃, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₁–C₁₈ alkoxy, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, substituted or unsubstituted aryl; and salts thereof, or a pharmaceutical composition thereof.
 12. The compound or salt of claim 1, wherein Y is OR₁, wherein R₁ is selected from H, C(═O)R′, P(═O)R′R″, S(═O)R′R″, substituted or unsubstituted C₁–C₁₈ alkyl, substituted or unsubstituted C₂–C₁₈ alkenyl, substituted or unsubstituted C₂–C₁₈ alkynyl, or substituted or unsubstituted aryl and wherein the dotted line indicates an optional double bond such that Y can also be ═O.
 13. The compound or salt of claim 1, wherein wherein Y is OH, O(C═O)R′ where R′ is optionally halogen-substituted alkyl, OP(═O)R′₂ where R′ is alkoxy, NH₂, ═O, ═NOH. 